US5763616A - Indazolesulfonylurea derivative, its use and intermediate for its production - Google Patents
Indazolesulfonylurea derivative, its use and intermediate for its production Download PDFInfo
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- US5763616A US5763616A US08/779,437 US77943797A US5763616A US 5763616 A US5763616 A US 5763616A US 77943797 A US77943797 A US 77943797A US 5763616 A US5763616 A US 5763616A
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/06—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
- C07D231/54—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings condensed with carbocyclic rings or ring systems
- C07D231/56—Benzopyrazoles; Hydrogenated benzopyrazoles
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- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
- A01N47/28—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N<
- A01N47/36—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N< containing the group >N—CO—N< directly attached to at least one heterocyclic ring; Thio analogues thereof
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D521/00—Heterocyclic compounds containing unspecified hetero rings
Definitions
- the present invention relates to a novel indazolesulfonylurea derivative (hereinafter referred to as a compound of the present invention), an intermediate for its production and a herbicide containing it as an active ingredient.
- a novel indazolesulfonylurea derivative hereinafter referred to as a compound of the present invention
- sulfonylurea derivatives such as sulfometuron-methyl have been known as herbicides.
- Japanese Unexamined Patent Publication No. 95091/1992 discloses a herbicide containing an indazolesulfonylurea as an active ingredient.
- the compound of the present invention i.e. a sulfonylurea derivative having a sulfamoyl group substituted at the 3-position of an indazole ring
- the intermediate for its production i.e. an indazolesulfonamide derivative, has also not been known.
- the present inventors have conducted various studies, and as a result, they have found that the compound of the present invention is an excellent herbicide having a high activity and has finally accomplished the present invention.
- the present invention provides an indazolesulfonylurea derivative represented by the general formula: ##STR2## ⁇ wherein R 1 is a hydrogen atom, an alkyl group, a cycloalkyl group, a haloalkyl group, an alkoxyalkyl group, a benzyloxyalkyl group, a benzyl group, a phenyl group, a pyridyl group, a dialkylaminocarbonyl group, an alkoxycarbonyl group, an alkylsulfonyl group, a phenylsulfonyl group, a dialkylaminosulfonyl group, a haloalkylcarbonyl group, an alkylcarbonyl group, a benzoyl group or an alkenyl group, R 2 and R 3 are the same or different and represent a hydrogen atom, a halogen atom, an alkyl group, a cycloalkyl group,
- R 1 is a hydrogen atom, an alkyl group, a cycloalkyl group, a haloalkyl group, an alkoxyalkyl group, a benzyloxyalkyl group, a benzyl group, a phenyl group, a pyridyl group, a dialkylaminocarbonyl group, an alkoxycarbonyl group, an alkylsulfonyl group, a phenylsulfonyl group, a dialkylaminosulfonyl group, a haloalkylcarbonyl group, an alkylcarbonyl group, a benzoyl group or an alkenyl group
- R 2 and R 3 are the same or different and represent a hydrogen atom, a halogen atom, an alkyl group, a cycloalkyl group, an alkenyl group, an alkoxycarbonylalkenyl
- the compound of the present invention includes a tautomer, a geometrical isomer and an optical isomer thereof.
- the alkyl group means a straight chain or branched chain alkyl group having from 1 to 30 carbon atoms and includes, for example, a methyl group, an ethyl group, a n-propyl group, an isopropyl group, a n-butyl group, an isobutyl group, a sec-butyl group, a t-butyl group, a n-pentyl group, an isoamyl group, a neopentyl group, a n-hexyl group, an isohexyl group, a 3,3-dimethylbutyl group, a n-heptyl group, a 5-methylhexyl group, a 4-methylhexyl group, a 3-methylhexyl group, a 4,4-dimethylpentyl group, a n-octyl group, a 6-methylheptyl group, a n-non
- alkoxy group and the alkylsulfonyl group mean an (alkyl)--O-- group and and (alkyl)--SO 2 -- group, respectively, in which the alkyl moiety has the above-mentioned meaning.
- the halogen atom includes fluorine, chlorine, bromine and iodine atoms.
- the alkenyl group means a straight chain or branched chain alkenyl group having from 2 to 20 carbon atoms and includes, for example, a vinyl group, a propenyl group, an isopropenyl group, a butenyl group, a pentenyl group, a hexenyl group, a heptenyl group, an octenyl group, a 3-methyl-1-butenyl group, and a 4-methyl-1-pentenyl group.
- the alkynyl group means a straight chain or branched chain alkynyl group having from 2 to 20 carbon atoms and includes, for example, an ethynyl group, a propynyl group, a butynyl group, a pentynyl group, a hexynyl group, a 3,3-dimethyl-1-butynyl group, a 4-methyl-1-pentynyl group, a 3-methyl-1-pentynyl group, a 5-methyl-1-hexynyl group, a 4-methyl-1-hexynyl group, a 3-methyl-1-hexynyl group, a heptynyl group, an octynyl group, a nonynyl group, a decynyl group, an undecynyl group, a dodecynyl group, a tridecynyl group, a tetradecy
- R 1 represents a hydrogen atom, a methyl group or an ethyl group
- R 2 and R 3 are the same or different and represent a hydrogen atom, a halogen atom, an alkoxycarbonyl group, a dialkylaminocarbonyl group, an alkoxy group, a haloalkoxy group, an alkenyloxy group, a cyano group or a trifluoromethyl group
- a and B are the same or different and represent a methoxy group, a methyl group or a haloalkoxy group
- Z represents a methine group or a nitrogen atom
- X represents an oxygen atom
- Y represents a hydrogen atom.
- the compound of the present invention represented by the formula I! or II! can be produced by reacting an intermediate for its production of the present invention represented by the formula I-a! or II-a! (hereinafter referred to as an intermediate, and the process for its production will be described hereinafter) and a compound represented by the formula III!.
- This reaction is usually conducted in a solvent or without solvent, if necessary, in the presence of a base.
- the range of the reaction temperature is a range from -20° C. to the boiling point of the solvent, and the range of the reaction time is a range of from 0.5 hour to 24 hours.
- the amounts of the compounds to be subjected to the reaction are respectively independently from 1 to 1.5 equivalent relative to one equivalent of the intermediate represented by the formula I-a! or II-a!.
- an aromatic hydrocarbon such as benzene, xylene or toluene, a halogenated hydrocarbon such as chloroform, carbon tetrachloride, dichloroethane, chlorobenzene or dichlorobenzene
- an ether such as diethyl ether, dioxane, tetrahydrofuran (THF), isopropyl ether (IPE) or diethylene glycol dimethyl ether
- an alcohol such as methanol, ethanol or 2-propanol
- an ester such as ethyl acetate or butyl acetate
- a nitro compound such as nitromethane or nitrobenzene
- a nitrile such as acetonitrile or isobutyronitrile
- an aprotic polar solvent such as formamide, N,N-dimethylformamide (DMF), N,N-dimethylacetamide (DMAC), dimethylsulfoxide (DMSO) or N
- an organic base such as pyridine, triethylamine, 1,4-diazabicyclo 2.2.2!octane, 1,8-diazabicyclo 5.4.0!-7-undecene (DBU), N,N-diethylaniline or diethyl-methylamine
- an inorganic base such as sodium hydroxide, potassium hydroxide, sodium carbonate, potassium carbonate or sodium hydride, or an alkali metal alkoxide such as sodium methoxide or sodium ethoxide, may, for example, be mentioned.
- the compound represented by the formula III! can be produced by reacting a compound represented by the formula IV! in Process 2 with phenyl chloroformate, phenyl chlorothio-O-formate or phenyl chlorodithioformate, in a proper solvent in the presence of a base.
- phenyl chloroformate phenyl chlorothio-O-formate
- phenyl chlorodithioformate phenyl chlorodithioformate
- the compound of the present invention represented by the formula I! or II! can be produced by reacting a compound represented by the formula I-b! or II-b! and a compound represented by the formula IV!.
- the compound represented by the formula I-b! or II-b! can be produced by reacting an intermediate represented by the formula I-a! or II-a! with phosgene or thiophosgene in a suitable solvent.
- This reaction is usually conducted in a solvent or without solvent, if necessary, in the presence of a base.
- the range of the reaction temperature, the range of the reaction time, and the solvent and the base to be used in the reaction are the same as in Process 1.
- the amounts of the compounds to be subjected to the reaction are respectively independently from 1 to 1.5 equivalent relative to one equivalent of the compound represented by the formula I-b! or II-b!.
- the compound of the present invention represented by the formula I! or II! can be produced by reacting a compound represented by the formula I-c! or II-c! and a compound of the formula IV!.
- the compound represented by the formula I-c! or II-c! can be produced by reacting an intermediate represented by the formula I-a! or II-a! with phenyl chloroformate, phenyl chlorothio-O-formate or phenyl chlorodithioformate, in a suitable solvent in the presence of a base. It may also be produced by reacting a compound represented by the formula I-b! or II-b! with phenol or thiophenol.
- This reaction is usually conducted in a solvent or without solvent, if necessary, in the presence of a base.
- the range of the reaction temperature, the range of the reaction time, and the solvent and the base to be used in the reaction are the same as in Process 1.
- the amounts of the compounds to be subjected to the reaction are respectively independently from 1 to 1.5 equivalent relative to one equivalent of the compound represented by the formula I-c! or II-c!.
- a process for producing an intermediate of the formula I-a! useful for the production of the compound of the present invention will be shown by Process 1 For Producing An Intermediate, and a process for producing an intermediate of the formula II-a! will be shown by Process 2 For Producing An Intermediate.
- a compound represented by the formula V! is reacted with the corresponding hydrazine derivative, for example, in DMSO, to obtain a compound represented by the formula VI!.
- a diazonium salt is formed, and this is reacted with sulfurous acid gas in a solvent such as acetic acid in the presence of copper chloride to obtain a compound represented by the formula VII!.
- This is reacted with excess t-butylamine to produce a compound represented by the formula I-d!.
- the t-butyl group is removed with excess trifluoroacetic acid to obtain an intermediate represented by the formula I-a!.
- R 1 represents an alkyl group, a haloalkyl group, a benzyl group or a phenyl group
- R 2 and R 3 represent a hydrogen atom, an alkyl group, a halogen atom, an alkoxy group, a phenyl group, a benzyl group or a haloalkoxy group.
- a compound represented by the formula IX! can be produced by reacting a compound represented by the formula VIII! with n-butyl lithium, for example, in ethyl ether, within a temperature range of from -40° to -20° C., followed by blowing in sulfurous acid gas.
- An intermediate represented by the formula II-a! can be produced by adding an aqueous solution of the compound represented by the formula IX! to an aqueous solution of a mixture of hydroxylamine-o-sulfonic acid and a base under cooling with ice.
- the compound of the formula VIII! can be produced by a method disclosed in a known literature such as Liebigs Ann. Chem., 908 (1980)!, Org. Synth. Coll. Vol. V, 650!, J. Chem. Soc. Perkin Trans. II, 1695, (1975)!, or Org. Synth, Coll. Vol. V, 941!.
- the intermediate represented by the formula I-a! or II-a! can be produced also by the following process.
- R 1 represents an alkyl group, a cycloalkyl group, a haloalkyl group, an alkoxyalkyl group, a benzyloxyalkyl group, a benzyl group, a dialkylaminocarbonyl group, an alkoxycarbonyl group, a alkylsulfonyl group, a phenylsulfonyl group, a dialkylaminosulfonyl group, a haloalkylcarbonyl group, an alkylcarbonyl group, a benzoyl group or an alkenyl group
- R 2 or R 3 represents a hydrogen atom, a halogen atom, an alkoxy group, a haloalkoxy group, a haloalkyl group, an alkoxycarbonyl group, a phenyl group or a
- a compound represented by the formula X! is reacted with N-bromosuccinimide, N-chlorosuccinimide, or bromine or chlorine in carbon tetrachloride in the presence of a light and a radical reaction initiating agent to obtain a compound represented by the formula XI!.
- the compound represented by the formula XI! is reacted with thiourea to obtain a compound represented by the formula XII!.
- the compound represented by the formula XII! is reacted with chlorine or bromine in a mixed solution of acetic acid and water to obtain a compound represented by the formula XIII!.
- this compound is reacted with t-butylamine to obtain a compound represented by the formula XIV!.
- the compound represented by the formula XIV! is reduced to obtain a compound represented by the formula XV!.
- the compound represented by the formula XV! and isoamylnitrous acid are reacted, followed by reaction with hydrochloric acid to obtain a compound represented by the formula XVI!.
- the compound represented by the formula XVI! is reacted with e.g. an alkyl halide or a benzyl halide to obtain a compound represented by the formula I-d! or II-d!.
- the compound represented by the formula XVI!, I-d! or II-d! can be converted to a compound represented by the formula XVII! and an intermediate represented by the formula I-a! or II-a!, respectively, by removing the t-butyl group with trifluoroacetic acid, as shown in Process 1 For Producing An Intermediate.
- the intermediate represented by the formula I-a! may be prepared by various processes depending upon the types of the substituents. However, it can be produced by the processes represented by the following Process 4 For Producing An Intermediate and Processes 5-1 to 5-3 For Producing An Intermediate. ##STR71## (wherein R 1 represents a hydrogen atom, an alkyl group, a benzyl group or a phenyl group, R 2 represents a halogen atom, preferably a fluorine atom, R 3 has the same meaning as defined above, and R 4 represents an alkoxy group, an alkoxyalkoxy group, a benzyloxy group, a cycloalkylalkoxy group, a haloalkoxy group, a dialkylaminoalkoxy group, an alkylthio group, an alkylamino group, a dialkylamino group or a benzylamino group.)
- an intermediate represented by the formula I-a! or II-a! is reacted with a compound represented by the formula R 4 -H (wherein R 4 has the same meaning as defined above) in a polar solvent such as DMSO, DMF, DMAC or NMP in the presence of a base such as sodium hydride, potassium hydride, potassium carbonate, potassium t-butoxide, sodium hydroxide or potassium hydroxide, to obtain an intermediate represented by the formula I-e! or II-e!, respectively.
- a polar solvent such as DMSO, DMF, DMAC or NMP
- a base such as sodium hydride, potassium hydride, potassium carbonate, potassium t-butoxide, sodium hydroxide or potassium hydroxide
- R 1 represents an alkyl group, a benzyl group or a phenyl group
- R 3 has the same meaning as defined above
- R 5 represents an alkyl group, a benzyl group, an alkenyl group, an alkynyl group, a haloalkenyl group, a haloalkyl group, an alkoxyalkyl group, an alkoxycarbonylalkyl group or a cyanoalkyl group
- L 1 represents a halogen atom, an alkylsulfonyloxy group, a haloalkylsulfonyloxy group or a benzenesulfonyloxy group which may be substituted.
- the intermediate represented by the formula I-f! or II-f! can be produced by the following process.
- R 1 represents an alkyl group, a benzyl group or a phenyl group
- R 2 represents a halogen atom, preferably a fluorine atom
- R 3 represents a hydrogen atom, a halogen atom, an alkyl group, a haloalkyl group, a haloalkoxy group or an alkoxy group
- R 8 represents an alkyl group, a benzyl group or a cycloalkyl group, preferably a cyclopropylmethyl group.
- an intermediate represented by the formula I-f! or II-f! is reacted with acetal of DMF to obtain a compound represented by the formula I-i! or II-i!, which is then reacted with a compound represented by the formula R 5 -L 1 (wherein R 5 and L 1 have the same meanings as defined above) in a suitable solvent in the presence of a base to obtain a compound represented by the formula I-j! or II-j!, which is then hydrolyzed with an acid or alkali to obtain an intermediate represented by the formula I-g! or II-g!.
- a mixture comprising 62 g (221 mmol) of 4-cyclopropylmethoxy-2-methyl-2H-indazole-3-sulfonamide, 120 ml of acetic acid and 120 ml of concentrated hydrochloric acid, was stirred at 80° C. for one hour. After concentrating acetic acid-hydrochloric acid, the mixture was poured into ice water. Crystals were collected by filtration and washed with water. Further, the crystals were washed with IPE and dried to obtain 35.1 g (yield: 70%) of the desired product. Melting point: 180°-181° C.
- the herbicide of the present invention contains an indazolesulfonylurea derivative represented by the general formula I! or II! as an active ingredient.
- the compound of the present invention may be used by itself. However, it may be used in the form of a formulation such as a dust, a wettable powder, an emulsifiable concentrate, a microgranule or a granule by blending it with a carrier, a surfactant, a dispersant or an adjuvant which is commonly used for formulations.
- a formulation such as a dust, a wettable powder, an emulsifiable concentrate, a microgranule or a granule by blending it with a carrier, a surfactant, a dispersant or an adjuvant which is commonly used for formulations.
- the carrier to be used for such formulations may, for example, be a solid carrier such as Zeeklite, talc, bentonite, clay, kaolin, diatomaceous earth, fine silica, vermiculite, calcium carbonate, slaked lime, silica sand, ammonium sulfate or urea, or a liquid carrier such as isopropyl alcohol, xylene, cyclohexane or methylnaphthalene.
- a solid carrier such as Zeeklite, talc, bentonite, clay, kaolin, diatomaceous earth, fine silica, vermiculite, calcium carbonate, slaked lime, silica sand, ammonium sulfate or urea
- a liquid carrier such as isopropyl alcohol, xylene, cyclohexane or methylnaphthalene.
- a metal salt of alkylbenzenesulfonic acid, a metal salt of dinaphthylmethane disulfonic acid, a salt of alcohol-sulfuric acid ester, an alkylaryl sulfonate, a lignin sulfonate, a polyoxyethylene glycol ether, a polyoxyethylene alkylaryl ether or a polyoxyethylene sorbitol monoalkylate may, for example, be mentioned.
- the adjuvant may, for example, be carboxymethyl cellulose, polyethylene glycol or gum arabic.
- the herbicide may be diluted to a suitable concentration before application, or may be directly applied.
- the herbicide of the present invention may be used for application to foliage, soil or water surface.
- the blending proportion of the active ingredient is suitably selected as the case requires. However, in a case of a dust or a granule, the proportion of the active ingredient is selected suitably within a range of from 0.01 to 10% (by weight), preferably from 0.05 to 5% (by weight). In a case of an emulsifiable concentrate or a wettable powder, the proportion is selected suitably within a range of from 1 to 50% (by weight), preferably from 5 to 30% (by weight).
- the dose of the herbicide of the present invention varies depending upon the type of the compound, the weeds to be controlled, the germination tendency, the environmental conditions and the type of the formulation to be used.
- the dose of the active ingredient is selected suitably within a range of from 0.1 g to 5 kg, preferably from 1 g to 1 kg, per 10 ares.
- the dose of the active ingredient is selected suitably within a range of from 0.1 to 50,000 ppm, preferably from 10 to 10,000 ppm.
- the compound of the present invention may be used in combination with an insecticide, a fungicide, other herbicide, a plant growth controlling agent, a fertilizer or the like, as the case requires.
- the compound of the present invention represented by the general formula I! or II! is capable of controlling annual weeds such as barnyardgrass (Echinochloa oryzicola), smallflower umbrella-plant (Cyperus difformis) and monochoria (Monochoria vaginalis) as well as perennial weeds such as Japanese ribbon wapato (Sagittaria pygmaea), arrowhead (Sagittaria trifolia), water nutgrass (Cvperus serotinus), water chestnut (Eleocharis kuroquwai), bulrush (Scirpus juncoides) and narrow-leaved arrowhead (Alisma canaliculatum), which germinate in paddy fields.
- annual weeds such as barnyardgrass (Echinochloa oryzicola), smallflower umbrella-plant (Cyperus difformis) and monochoria (Monochoria vaginalis)
- perennial weeds such as Japanese ribbon wapato (Sagittaria
- weeds problematic in upland fields including broadleaf weeds such as smartweed (Polygonum lapathifolium), green amaranth (Amaranthus viridis), lambsquater (Chenopodium album), goose grass (Galium aparine), chickweed (Stellaria media), velvetleaf (Abtilon theophrasti), prickly sida (Sida spinosa), hemp sesbania (Sesbania exaltata), morningglory (Ipomoea spp) and common cocklebur (Xanthium strumarium), perennial and annual syperaceous weeds such as purple nutsedge (Cyperus rotundus), yellow nutsedge (Cyperus esculentus), himekugu (Cyperus brevifolius var.
- smartweed Polygonum lapathifolium
- green amaranth Amaranthus viridis
- lambsquater Chopodium album
- goose grass Galium aparine
- the herbicide of the present invention is highly safe to crop plants and exhibits particularly high safety to e.g. rice, wheat, barley, corn, grain sorghum and sugar beat.
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Abstract
The present invention provides an indazolesulfonylurea derivative represented by the general formula: <IMAGE> <IMAGE> [wherein R1 is a hydrogen atom or an alkyl group, etc., R2 and R3 are the same or different and represent a hydrogen atom, a halogen atom, an alkyl group, the formula -COR4 (wherein R4 represents an alkoxy group, etc.), an alkoxy group, a haloalkoxy group or a cyano group, etc., X is an oxygen atom or a sulfur atom, Y is a hydrogen atom or an alkyl group, etc., A and B are the same or different and represent a halogen atom, an alkoxy group or an alkyl group, etc., and Z represents a nitrogen atom or a methine group], as well as a herbicide containing it as an active ingredient and an intermediate for its production. The compound of the present invention exhibits excellent herbicidal effects over a wide range from the preemergence stage to the growing stage of various weeds which are problematic in agricultural fields. Further, it is capable of controlling weeds germinating in paddy fields.
Description
This is a Division of application Ser. No. 08/630,092 filed on Apr. 9, 1996, now U.S. Pat. No. 5,670,452, which is a Division of application Ser. No. 08/373,273 filed on Jan. 30, 1995, now U.S. Pat. No. 5,534,481, which was originally filed as International Application No. PCT/JP94/01016 filed on Jun. 24, 1994.
The present invention relates to a novel indazolesulfonylurea derivative (hereinafter referred to as a compound of the present invention), an intermediate for its production and a herbicide containing it as an active ingredient.
Heretofore, many sulfonylurea derivatives such as sulfometuron-methyl have been known as herbicides. Japanese Unexamined Patent Publication No. 95091/1992 discloses a herbicide containing an indazolesulfonylurea as an active ingredient. However, the compound of the present invention i.e. a sulfonylurea derivative having a sulfamoyl group substituted at the 3-position of an indazole ring, has not been known. Further, the intermediate for its production i.e. an indazolesulfonamide derivative, has also not been known.
It is known that sulfonylurea derivatives have herbicidal activities, but such compounds are not necessarily practically satisfactory, for example, in that their herbicidal effects are inadequate.
Under these circumstances, the present inventors have conducted various studies, and as a result, they have found that the compound of the present invention is an excellent herbicide having a high activity and has finally accomplished the present invention.
Namely, the present invention provides an indazolesulfonylurea derivative represented by the general formula: ##STR2## {wherein R1 is a hydrogen atom, an alkyl group, a cycloalkyl group, a haloalkyl group, an alkoxyalkyl group, a benzyloxyalkyl group, a benzyl group, a phenyl group, a pyridyl group, a dialkylaminocarbonyl group, an alkoxycarbonyl group, an alkylsulfonyl group, a phenylsulfonyl group, a dialkylaminosulfonyl group, a haloalkylcarbonyl group, an alkylcarbonyl group, a benzoyl group or an alkenyl group, R2 and R3 are the same or different and represent a hydrogen atom, a halogen atom, an alkyl group, a cycloalkyl group, an alkenyl group, an alkoxycarbonylalkenyl group, an alkynyl group, a haloalkyl group, an alkoxyalkyl group, an alkoxycarbonylalkyl group, an alkylcarbonylalkyl group, a cycloalkylcarbonylalkyl group, a cyanoalkyl group, a dialkylaminocarbonylalkyl group, a dialkylaminoalkyl group, a dialkylaminosulfonylalkyl group, an azidoalkyl group, a benzyl group, a phenyl group, a nitro group, a cyano group, an azide group, an amino group, a monoalkylamino group, a dialkylamino group, a benzylamino group, an alkylcarbonylamino group which may be substituted by a halogen atom, a benzoylamino group, an alkoxycarbonylamino group, a phenoxycarbonylamino group, an alkylsulfonylamino group wherein the amino group may be substituted by an alkyl group, a phenylsulfonylamino group wherein the amino group may be substituted by an alkyl group, an alkylideneamino group, a benzylideneamino group, a tetrazolyl group which may be substituted, a group represented by the formula --COR4 (wherein R4 is a hydrogen atom, a hydroxyl group, an alkyl group, a cycloalkyl group, a haloalkyl group, an alkenyl group, an alkynyl group, a benzyl group, a phenyl group, an alkoxy group, a haloalkoxy group, an alkoxyalkoxy group, an alkenyloxy group, a haloalkenyloxy group, an alkynyloxy group, a benzyloxy group or a phenoxy group), a group represented by the formula --C(O)NR5 R6 (wherein R5 and R6 are the same or different and represent a hydrogen atom, an alkyl group, an alkenyl group, an alkynyl group, a benzyl group, a phenyl group or an alkoxy group), a group represented by the formula --SR7 (wherein R7 is a hydrogen atom, an alkyl group or a haloalkyl group), a group represented by the formula --SO2 NR5 R6 (wherein R5 and R6 have the same meanings as defined above), a group represented by the formula --S(O)n R8 (wherein n represents an integer of 1 or 2, and R8 represents an alkyl group, an alkenyl group or a haloalkyl group), a group represented by the formula --OR9 wherein R9 is a hydrogen atom, an alkyl group, a cycloalkylalkyl group, an alkenyl group, an alkynyl group, a benzyl group (said group may be substituted by a halogen atom, an alkyl group or an alkoxy group), a haloalkyl group, a haloalkenyl group, a phenyl group (said group may be substituted by a halogen atom, an alkyl group or an alkoxy group), an alkoxyalkyl group, an alkoxyalkoxyalkyl group, a haloalkoxyalkyl group, a benzyloxyalkyl group, a phenoxyalkyl group, an alkylthioalkyl group, a dialkylaminoalkyl group, an azidoalkyl group, an alkylcarbonyl group, a haloalkylcarbonyl group, a benzoyl group, a dialkylaminocarbonyl group, a cyanoalkyl group, an alkylideneamino group, a dialkylideneamino group, a benzylideneamino group or an alkoxycarbonylalkyl group!, or the formula --C(═NOR10)R11 (wherein R10 represents a hydrogen atom, an alkyl group, an alkenyl group, an alkynyl group, a benzyl group, a haloalkyl group or a phenyl group, and R11 represents a hydrogen atom, an alkyl group, a benzyl group, a haloalkyl group or a phenyl group), R2 and R3 may together form a ring with an alkyl group which may contain a hetero atom, A and B are the same or different and represent an alkyl group, a haloalkyl group, an alkoxy group, a monoalkylamino group, a dialkylamino group, a halogen atom or a haloalkoxy group, Z represents a methine group or a nitrogen atom, X represents an oxygen atom or a sulfur atom, and Y represents a hydrogen atom, an alkyl group or an alkoxyalkyl group, as well as its intermediate represented by an indazolesulfonamide derivative represented by the formula I-a! or II-a!: ##STR3## {wherein R1 is a hydrogen atom, an alkyl group, a cycloalkyl group, a haloalkyl group, an alkoxyalkyl group, a benzyloxyalkyl group, a benzyl group, a phenyl group, a pyridyl group, a dialkylaminocarbonyl group, an alkoxycarbonyl group, an alkylsulfonyl group, a phenylsulfonyl group, a dialkylaminosulfonyl group, a haloalkylcarbonyl group, an alkylcarbonyl group, a benzoyl group or an alkenyl group, R2 and R3 are the same or different and represent a hydrogen atom, a halogen atom, an alkyl group, a cycloalkyl group, an alkenyl group, an alkoxycarbonylalkenyl group, an alkynyl group, a haloalkyl group, an alkoxyalkyl group, an alkoxycarbonylalkyl group, an alkylcarbonylalkyl group, a cycloalkylcarbonylalkyl group, a cyanoalkyl group, a dialkylaminocarbonylalkyl group, a dialkylaminoalkyl group, a dialkylaminosulfonylalkyl group, an azidoalkyl group, a benzyl group, a phenyl group, a nitro group, a cyano group, an azide group, an amino group, a monoalkylamino group, a dialkylamino group, a benzylamino group, an alkylcarbonylamino group which may be substituted by a halogen atom, a benzoylamino group, an alkoxycarbonylamino group, a phenoxycarbonylamino group, an alkylsulfonylamino group wherein the amino group may be substituted by an alkyl group, a phenylsulfonylamino group wherein the amino group may be substituted by an alkyl group, an alkylideneamino group, a benzylideneamino group, a tetrazolyl group which may be substituted, a group represented by the formula --COR4 (wherein R4 is a hydrogen atom, a hydroxyl group, an alkyl group, a cycloalkyl group, a haloalkyl group, an alkenyl group, an alkynyl group, a benzyl group, a phenyl group, an alkoxy group, a haloalkoxy group, an alkoxyalkoxy group, an alkenyloxy group, a haloalkenyloxy group, an alkynyloxy group, a benzyloxy group or a phenoxy group), a group represented by the formula --C(O)NR5 R6 (wherein R5 and R6 are the same or different and represent a hydrogen atom, an alkyl group, an alkenyl group, an alkynyl group, a benzyl group, a phenyl group or an alkoxy group), a group represented by the formula --SR7 (wherein R7 is a hydrogen atom, an alkyl group or a haloalkyl group), a group represented by the formula --SO2 NR5 R6 (wherein R5 and R6 have the same meanings as defined above), a group represented by the formula --S(O)n R8 (wherein n represents an integer of 1 or 2, and R8 represents an alkyl group, an alkenyl group or a haloalkyl group), a group represented by the formula --OR9 wherein R9 is a hydrogen atom, an alkyl group, a cycloalkylalkyl group, an alkenyl group, an alkynyl group, a benzyl group (said group may be substituted by a halogen atom, an alkyl group or an alkoxy group), a haloalkyl group, a haloalkenyl group, a phenyl group (said group may be substituted by a halogen atom, an alkyl group or an alkoxy group), an alkoxyalkyl group, an alkoxyalkoxyalkyl group, a haloalkoxyalkyl group, a benzyloxyalkyl group, a phenoxyalkyl group, an alkylthioalkyl group, a dialkylaminoalkyl group, an azidoalkyl group, an alkylcarbonyl group, a haloalkylcarbonyl group, a benzoyl group, a dialkylaminocarbonyl group, a cyanoalkyl group, an alkylideneamino group, a dialkylideneamino group, a benzylideneamino group or an alkoxycarbonylalkyl group!, or the formula --C(═NOR10)R11 (wherein R10 represents a hydrogen atom, an alkyl group, an alkenyl group, an alkynyl group, a benzyl group, a haloalkyl group or a phenyl group, and R11 represents a hydrogen atom, an alkyl group, a benzyl group, a haloalkyl group or a phenyl group), and R2 and R3 may form a ring with an alkyl group which may contain a hetero atom}, and a herbicide containing the indazolesulfonylurea as an active ingredient.
The compound of the present invention includes a tautomer, a geometrical isomer and an optical isomer thereof.
In the present invention, the alkyl group means a straight chain or branched chain alkyl group having from 1 to 30 carbon atoms and includes, for example, a methyl group, an ethyl group, a n-propyl group, an isopropyl group, a n-butyl group, an isobutyl group, a sec-butyl group, a t-butyl group, a n-pentyl group, an isoamyl group, a neopentyl group, a n-hexyl group, an isohexyl group, a 3,3-dimethylbutyl group, a n-heptyl group, a 5-methylhexyl group, a 4-methylhexyl group, a 3-methylhexyl group, a 4,4-dimethylpentyl group, a n-octyl group, a 6-methylheptyl group, a n-nonyl group, a 7-methyloctyl group, a n-decyl group, a 8-methylnonyl group, a n-undecyl group, a 9-methyldecyl group, a n-dodecyl group, a 10-methylundecyl group, a n-tridecyl group, a 11-methyldodecyl group, a n-tetradecyl group, a 12-methyltridecyl group, a n-pentadecyl group, a 13-methyl-tetradecyl group, a n-hexadecyl group, a n-heptadecyl group, a n-octadecyl group, a n-nonadecyl group, and a n-eicosyl group.
The alkoxy group and the alkylsulfonyl group mean an (alkyl)--O-- group and and (alkyl)--SO2 -- group, respectively, in which the alkyl moiety has the above-mentioned meaning.
The halogen atom includes fluorine, chlorine, bromine and iodine atoms.
The alkenyl group means a straight chain or branched chain alkenyl group having from 2 to 20 carbon atoms and includes, for example, a vinyl group, a propenyl group, an isopropenyl group, a butenyl group, a pentenyl group, a hexenyl group, a heptenyl group, an octenyl group, a 3-methyl-1-butenyl group, and a 4-methyl-1-pentenyl group.
The alkynyl group means a straight chain or branched chain alkynyl group having from 2 to 20 carbon atoms and includes, for example, an ethynyl group, a propynyl group, a butynyl group, a pentynyl group, a hexynyl group, a 3,3-dimethyl-1-butynyl group, a 4-methyl-1-pentynyl group, a 3-methyl-1-pentynyl group, a 5-methyl-1-hexynyl group, a 4-methyl-1-hexynyl group, a 3-methyl-1-hexynyl group, a heptynyl group, an octynyl group, a nonynyl group, a decynyl group, an undecynyl group, a dodecynyl group, a tridecynyl group, a tetradecynyl group, a pentadecynyl group, and a hexadecynyl group.
In the above formula I! or II!, as a group of compounds showing preferred herbicidal effects, compounds may be mentioned wherein R1 represents a hydrogen atom, a methyl group or an ethyl group, R2 and R3 are the same or different and represent a hydrogen atom, a halogen atom, an alkoxycarbonyl group, a dialkylaminocarbonyl group, an alkoxy group, a haloalkoxy group, an alkenyloxy group, a cyano group or a trifluoromethyl group, A and B are the same or different and represent a methoxy group, a methyl group or a haloalkoxy group, Z represents a methine group or a nitrogen atom, X represents an oxygen atom, and Y represents a hydrogen atom.
Now, typical specific examples of the compound of the present invention represented by the formula I! or II! will be exemplified in Tables 1 and 2. The compound numbers will be referred to in the subsequent description, and when R1 represents a hydrogen atom, the compound may take tautomers represented by the formula I! and II!.
The following symbols in the Tables in the present specification represent the following groups, respectively.
______________________________________
Bn: Benzyl group Pr: n-Propyl group
Pen: n-Pentyl group
Bu: n-Butyl group
Me: Methyl group Ph: Phenyl group
Et: Ethyl group
______________________________________
TABLE 1
__________________________________________________________________________
##STR4##
Comp.
No. R.sup.1 R.sup.2 R.sup.3 X Y A B Z mp.
__________________________________________________________________________
(°C.)
I-1 Me Ph H O H OMe OMe CH
I-2 Me Bn H O H OMe OMe CH
I-3 Me SH H O H OMe OMe CH
I-4 Me SMe H O H OMe OMe CH
I-5 Me SEt H O H OMe OMe CH 189-190
I-6 Me SPr H O H OMe OMe CH 162-164
I-7 Me SO.sub.2 Me
H O H OMe DMe CH
I-8 Me SO.sub.2 Et
H O H OMe OMe CH 157-160
I-9 Me SOMe H O H OMe OMe CH
I-10
Me SO.sub.2 NHMe
H O H OMe OMe CH
I-11
Me SO.sub.2 NHOMe
H O H OMe OMe CH
I-12
Me SO.sub.2 NMe.sub.2
H O H OMe OMe CH 214-216
I-13
Me SO.sub.2 NHBn
H O H OMe OMe CH
I-14
Me SO.sub.2 NHPh
H O H OMe OMe CH
I-15
Me SO.sub.2 NHCH.sub.2 CHCH.sub.2
H O H OMe OMe CH
I-16
Me SO.sub.2 NHCH.sub.2 CCH
H O H OMe OMe CH
I-17
H Cl H O H OMe OMe CH 191-193
I-18
Me Cl H O H Me Me CH 195-198
I-19
Me Cl 5-Cl O H OMe OMe CH 210-213
I-20
Et Cl H O H OMe OMe CH 187-189
I-21
Ph Cl H O H OMe OMe CH
I-22
Bn Cl H O H OMe OMe CH
I-23
Me H H O H OMe OMe CH 181-183
I-24
Me H H O H Me Me CH
I-25
Me H H O H OMe Me N 172-174
I-26
Me F H O H OMe OMe CH 205-209
I-27
Me Br H O H OMe OMe CH 276-279
I-28
Me Me H O H OMe OMe CH 178-180
I-29
Me CN H O H OMe OMe CH 267-269
I-30
Me CF.sub.3 H O H OMe OMe CH
I-31
Me Cl H O H OMe Me CH 243-245
I-32
Me Cl H O H OMe Me N 266-267
I-33
Me F H O H Me Me CH 195-197
I-34
Me F H O H OMe Me N 197-200
I-35
Me F H O H OMe Me CH 180-185
I-36
Me H 5-Cl O H OMe OMe CH
I-37
Me H 5-Cl O H Me Me CH
I-38
Me H 5-Cl O H OMe Me N
I-39
Me H 6-Cl O H OMe OMe CH
I-40
Me H 6-Cl O H Me Me CH
I-41
Me H 6-Cl O H OMe Me N
I-42
Me H 7-Cl O H OMe OMe CH
I-43
Me H 7-Cl O H OMe Me N
I-44
Me Cl H S H OMe OMe CH
I-45
Me Cl H O Me OMe OMe CH
I-46
Me COH H O H OMe OMe CH
I-47
Me COMe H O H OMe OMe CH
I-48
Me COEt H O H OMe OMe CH
I-49
Me COPh H O H OMe OMe CH
I-50
Me COCH.sub.2 CHCH.sub.2
H O H OMe OMe CH
I-51
Me COCH.sub.2 CCH
H O H OMe OMe CH
I-52
Me COBn H O H OMe OMe CH
I-53
Me NO.sub.2 H O H OMe OMe CH 219-220
I-54
Me NH.sub.2 H O H OMe OMe CH
I-55
Me NHMe H O H OMe OMe CH
I-56
Me NMe.sub.2 H O H OMe OMe CH
I-57
Me NHCOMe H O H OMe OMe CH
I-58
Me NHCOPh H O H OMe OMe CH
I-59
Me NHCOCH.sub.2 Cl
H O H OMe OMe CH
I-60
Me NHSO.sub.2 CH.sub.3
H O H OMe OMe CH
I-61
Me NHSO.sub.2 Ph
H O H OMe OMe CH
I-62
Me CO.sub.2 H H O H OMe OMe CH
I-63
Me CO.sub.2 Me
H O H OMe OMe CH 187-190
I-64
Me CO.sub.2 Et
H O H OMe OMe CH 192-195
I-65
Me CO.sub.2 Pr
H O H OMe OMe CH 195-197
I-66
Me CO.sub.2 Pr-i
H O H OMe OMe CH 168-169
I-67
Me CO.sub.2 Bu
H O H OMe OMe CH 169-172
I-68
Me CO.sub.2 Pen
H O H OMe OMe CH
I-69
Me CO.sub.2 Bn
H O H OMe OMe CH
I-70
Me CO.sub.2 Ph
H O H OMe OMe CH
I-71
Me CO.sub.2 CH.sub.2 CH.sub.2 F
H O H OMe OMe CH
I-72
Me CO.sub.2 CH.sub.2 CHCH.sub.2
H O H OMe OMe CH
I-73
Me CO.sub.2 CH.sub.2 CCH
H O H OMe OMe CH
I-74
Me CO.sub.2 Me
H O H OCHF.sub.2
OCHF.sub.2
CH
I-75
Me CO.sub.2 Et
H O H OCHF.sub.2
OCHF.sub.2
CH
I-76
Me CO.sub.2 Me
H O H OMe Cl CH
I-77
Me CO.sub.2 Me
H O H OMe Me CH
I-78
Me CO.sub.2 Me
H O H OMe Me N
I-79
Me CO.sub.2 Et
H O H OMe Me N 193-196
I-80
Me CO.sub.2 Me
H O H OMe OCHF.sub.2
CH
I-81
Me CO.sub.2 Me
5-F O H OMe OMe CH
I-82
Et CO.sub.2 Me
H O H OMe OMe CH 182-183
I-83
Bu CO.sub.2 Me
H O H OMe OMe CH
I-84
Bn CO.sub.2 Me
H O H OMe OMe CH
I-85
Ph CO.sub.2 Me
H O H OMe OMe CH
I-86
H CO.sub.2 Et
H O H OMe OMe CH
I-87
Me CO.sub.2 Me
H S H OMe OMe CH
I-88
Me CO.sub.2 Et
H S H OMe OMe CH
I-89
Me CO.sub.2 Me
H O Me OMe OMe CH
I-90
Me DH H O H OMe OMe CH
I-91
Me OMe H O H OMe OMe CH 265-267
I-92
Me OEt H O H OMe OMe CH 162-164
I-93
Me OPr H O H OMe OMe CH 134-136
I-94
Me OPr-i H O H OMe OMe CH 168-171
I-95
Me OBu H O H OMe OMe CH 198-200
I-96
Me OBn H O H OMe OMe CH
I-97
Me OBn(4-Cl) H O H OMe OMe CH
I-98
Me OBn(3-OMe) H O H OMe OMe CH
I-99
Me OBn(2-Me) H O H OMe OMe CH
I-100
Me OPh H O H OMe OMe CH
I-101
Me OPh(4-Cl) H O H OMe OMe CH
I-102
Me OPh(3-OMe) H O H OMe OMe CH
I-103
Me OPh(2-Me) H O H OMe OMe CH
I-104
Me OCH.sub.2 CHCH.sub.2
H O H OMe OMe CH
I-105
Me OCH.sub.2 CCH
H O H OMe OMe CH
I-106
Me OCH.sub.2 CF.sub.3
H O H OMe OMe CH
I-107
Me OCH.sub.2 CH.sub.2 OMe
H O H OMe OMe CH
I-108
Me OCH.sub.2 CH.sub.2 OPh
H O H OMe OMe CH
I-109
Me OCOMe H O H OMe OMe CH
I-110
Me OMe H O H OMe Me CH
I-111
Me OMe H O H OMe Me N 269-270
I-112
Me OMe H O H Me Me CH 267-268
I-113
Me OEt H O H OMe Cl CH 160-165
I-114
Me OEt H O H OMe Me CH 169-170
I-115
Me OEt H O H Me Me CH
I-116
Me CONH.sub.2 H O H OMe OMe CH
I-117
Me CONHMe H O H OMe OMe CH
I-118
Me CONHEt H O H OMe OMe CH
I-119
Me CONHPr H O H OMe OMe CH
I-120
Me CONMe.sub.2
H O H OMe OMe CH 205-207
I-121
Me CONEt.sub.2
H O H OMe OMe CH
I-122
Me CONHBn H O H OMe OMe CH
I-123
Me CONHPh H O H OMe OMe CH
I-124
Me CONHCH.sub.2 CHCH.sub.2
H O H OMe OMe CH
I-125
Me CONHCH.sub.2 CCH
H O H OMe OMe CH
I-126
Me CONHOMe H O H OMe OMe CH
I-127
Me H 5-F O H OMe OMe CH
I-128
Me H 5-F O H Me Me CH
I-129
Me H 5-F O H OMe Me CH
I-130
Me H 5-F O H OMe Me N
I-131
H COOMe H O H OMe OMe CH 179-180
I-132
H COOMe H O H OMe Cl CH 193-194
I-133
H Cl H O H OMe Cl CH 178-181
I-134
Me Cl H O H OMe OMe CH 265-267
I-135
Me SO.sub.2 NH.sub.2
H O H OMe OMe CH
I-136
H Br H O H OMe OMe CH 190-193
I-137
Me H 5-OMe O H OMe OMe CH
I-138
Me H 5-OEt O H OMe OMe CH
I-139
Me H 5-OPr O H OMe OMe CH
I-140
Me OCH(CF.sub.3)Me
H O H OMe OMe CH
I-141
Me OCH.sub.2 CH.sub.2 Cl
H O H OMe OMe CH
I-142
Me OCH.sub.2 CH.sub.2 F
H O H OMe OMe CH
I-143
Me OCH.sub.2 CH.sub.2 OEt
H O H OMe OMe CH
I-144
Me OCH.sub.2 CH.sub.2 OPr-i
H O H OMe OMe CH
I-145
Me OCH.sub.2 CH.sub.2 OBu
H O H OMe OMe CH
I-146
Me OCH.sub.2 CH.sub.2 OBu-t
H O H OMe OMe CH
I-147
Me OCH.sub.2 COOEt
H O H OMe OMe CH
I-148
Me OCH.sub.2 CH.sub.2 NMe.sub.2
H O H OMe OMe CH
I-149
Me SBu H O H OMe OM& CH 165-168
I-150
Me SPr-i H O H OMe OMe CH 178-180
I-151
Me SO.sub.2 Pr
H O H OMe OMe CH 163-167
I-152
Me SO.sub.2 Bu
H O H OMe OMe CH 187-189
I-153
Me SO.sub.2 Pr-i
H O H OMe OMe CH 279-281
I-154
Me NHBn H O H OMe OMe CH
I-155
Me NEt.sub.2 H O H OMe OMe CH
I-156
Me OMe 5-Cl O H OMe OMe CH
I-157
Me Br H O H OMe Me CH 276-279
I-158
Et Cl H O H OMe Me CH 182-184
I-159
Ph Cl H O H OMe Me CH
I-160
Me OPr H O H OMe Me CH 178-180
I-161
Me OBu H O H OMe Me CH 174-176
I-162
Me OPr-i H O H OMe Me CH 184-186
I-163
Me H 5-OMe O H OMe Me CH
I-164
Me H 5-OEt O H OMe Me CH
I-165
Me H 5-OPr O H OMe Me CH
I-166
Me OCH.sub.2 CF.sub.3
H O H OMe Me CH
I-167
Me OCH(CF.sub.3)Me
H O H OMe Me CH
I-168
Me OCH.sub.2 CH.sub.2 OMe
H O H OMe Me CH
I-169
Me OCH.sub.2 CH.sub.2 OEt
H O H OMe Me CH
I-170
Me OCH.sub.2 CH.sub.2 OPr-i
H O H OMe Me CH
I-171
Me OCH.sub.2 CH.sub.2 OBu
H O H OMe Me CH
I-172
Me OCH.sub.2 CH.sub.2 OBu-t
H O H OMe Me CH
I-173
Me OCH.sub.2 CH.sub.2 NMe.sub.2
H O H OMe Me CH
I-174
Me SPr H O H OMe Me CH 155-156
I-175
Me CO.sub.2 Pr
H O H OMe Me CH 185-186
I-176
Me CO.sub.2 Pr-i
H O H OMe Me CH 158-160
I-177
Me CO.sub.2 Bu
H O H OMe Me CH 174-175
I-178
Me NO.sub.2 H O H OMe Me CH 212-214
I-179
Me CN H O H OMe Me CH 180-181
I-180
Me Br H O H OMe Me N 166-169
I-181
Et Cl H O H OMe Me N 141-142
I-182
Me OPr H O H OMe Me N 210-213
I-183
Me OBu H O H OMe Me N 184-186
I-184
Me OPr-i H O H OMe Me N 157-159
I-185
Me H 5-OMe O H OMe Me N
I-186
Me H 5-OEt O H OMe Me N
I-187
Me H 5-OPr O H dMe Me N
I-188
Me OCH.sub.2 CF.sub.3
H O H OMe Me N
I-189
Me OCH.sub.2 CH.sub.2 OEt
H o H OMe Me N
I-190
Me OCH.sub.2 CH.sub.2 OPr-i
H O H OMe Me N
I-191
Me OCH.sub.2 CH.sub.2 OBu
H O H OMe Me N
I-192
Me OCH.sub.2 CH.sub.2 OBu-t
H O H OMe Me N
I-193
Me OCH.sub.2 CH.sub.2 NMe.sub.2
H O H OMe Me N
I-194
Me SEt H O H OMe Me N 223-224
I-195
Me SPr H O H OMe Me N
I-196
Me NMe.sub.2 H O H OMe Me N
I-197
Me CO.sub.2 Pr-i
H O H OMe Me N
I-198
Me CO.sub.2 Bu
H O H OMe Me N 177-178
I-199
Me CN H O H OMe Me N 255-258
I-200
Me OMe 5-Cl O H OMe Me N
I-201
Me Cl H O H Cl OMe CH
I-202
Et Cl H O H Cl OMe CH
I-203
Ph Cl H O H Cl OMe CH
I-204
Me OMe H O H Cl OMe CH 268-269
I-205
Me OPr H O H Cl OMe CH 168-169
I-206
Me OBu H O H Cl OMe CH 171-173
I-207
Me H 5-OMe O H Cl OMe CH
I-208
Me OCH.sub.2 CF.sub.3
H O H Cl OMe CH
I-209
Me SPr H O H Cl OMe CH 143-145
I-210
Me SBu H O H Cl OMe CH
I-211
Me SPr-i H O H Cl OMe CH 228-230
I-212
Me SO.sub.2 Pr-i
H O H Cl OMe CH 143-145
I-213
Me NHBn H O H Cl OMe CH
I-214
Me NMe.sub.2 H O H Cl OMe CH
I-215
Et Cl H O H Me Me CH
I-216
Me OPr H O H Me Me CH 149-150
I-217
Me OBu H O H Me Me CH 146-149
I-218
Me OPr-i H O H Me Me CH 174-176
I-219
Me NMe.sub.2 H O H Me Me CH
I-220
Me OMe H O H OMe OMe N
I-221
Me H 5-OEt O H OMe OMe N
I-222
Me H 5-OPr O H OMe OMe N
I-223
Me OCH.sub.2 CH.sub.2 OBu
H O H OMe OMe N
I-224
Me OCH.sub.2 CH.sub.2 OBu-t
H O H OMe OMe N
I-225
Me NHMe H O H OMe Me CH
I-226
Me NHMe H O H OMe Me N
I-227
Me OMe H O H OMe Me CH
I-228
Me OMe 5-OMe O H OMe Me CH
I-229
Me OCHF.sub.2 H O H OMe OMe CH 198-200
I-230
Me OCHF.sub.2 H O H Me OMe CH 177-179
I-231
Me OCHF.sub.2 H O H Me OMe N 165-167
I-232
Me OCH.sub.2 CHF.sub.2
H O H OMe OMe CH
I-233
Me OCH.sub.2 CHF.sub.2
H O H Me OMe CH
I-234
Me OCH.sub.2 CHF.sub.2
H O H Me OMe N
I-235
Me OCH.sub.2 CH.sub.2 CF.sub.3
H O H OMe OMe CH
I-236
Me OCH.sub.2 CH.sub.2 CF.sub.3
H O H Me OMe CH
I-237
Me OCH.sub.2 CH.sub.2 CF.sub.3
H O H Me OMe N
I-238
Me OCH(CF.sub.2 CF.sub.3)Me
H O H OMe OMe CH
I-239
Me OCH(CF.sub.2 CF.sub.3)Me
H O H Me OMe CH
I-240
Me OCH(CF.sub.2 CF.sub.3)Me
H O H Me OMe N
I-241
Me OCH.sub.2 CF.sub.2 CHF.sub.2
H O H OMe OMe CH
I-242
Me OCH.sub.2 CF.sub.2 CHF.sub.2
H O H Me OMe CH
I-243
Me OCH.sub.2 CF.sub.2 CHF.sub.2
H O H Me OMe N
I-244
Me OCH.sub.2 CF.sub.2 CF.sub.3
H O H OMe OMe CH
I-245
Me OCH.sub.2 CF.sub.2 CF.sub.3
H O H Me OMe CH
I-246
Me OCH.sub.2 CF.sub.2 CF.sub.3
H O H Me OMe N
I-247
Me OCH.sub.2 CHCl.sub.2
H O H OMe OMe CH
I-248
Me OCH.sub.2 CHCl.sub.2
H O H Me OMe CH
I-249
Me OCH.sub.2 CHCl.sub.2
H O H Me OMe N
I-250
Me OCF.sub.2 CH.sub.2 Cl
H O H OMe OMe CH
I-251
Me OCF.sub.2 CH.sub.2 Cl
H O H Me OMe CH
I-252
Me OCF.sub.2 CH.sub.2 Cl
H O H Me OMe N
I-253
Me OCF.sub.2 CHFCl
H O H OMe OMe CH
I-254
Me OCF.sub.2 CHFCl
H O H Me OMe CH
I-255
Me OCF.sub.2 CHFCl
H O H Me OMe N
I-256
Me OCF.sub.3 H O H OMe OMe CH
I-257
Me OCF.sub.3 H O H Me OMe CH
I-258
Me OCF.sub.3 H O H Me OMe N
I-259
Me OCH.sub.2 CHCHCl
H O H OMe OMe CH
I-260
Me OCH.sub.2 CHCHCl
H O H Me OMe CH
I-261
Me OCH.sub.2 CHCHCl
H O H Me OMe N
I-262
Me OCH.sub.2 CHCCl.sub.2
H O H OMe OMe CH
I-263
Me OCH.sub.2 CHCCl.sub.2
H O H Me OMe CH
I-264
Me OCH.sub.2 CHCCl.sub.2
H O H Me OMe N
I-265
Me OCH.sub.2 C(Cl)CH.sub.2
H O H OMe OMe CH
I-266
Me OCH.sub.2 C(Cl)CH.sub.2
H O H Me OMe CH
I-267
Me OCH.sub.2 C(Cl)CH.sub.2
H O H Me OMe N
I-268
Me OCH.sub.2 C(Me)CH.sub.2
H O H OMe OMe CH
I-269
Me OCH.sub.2 C(Me)CH.sub.2
H O H Me OMe CH
I-270
Me OCH.sub.2 C(Me)CH.sub.2
H O H Me OMe N
I-271
Me OCH.sub.2 CHCHMe
H O H OMe OMe CH
I-272
Me OCH.sub.2 CHCHMe
H O H Me OMe CH
I-273
Me OCH.sub.2 CHCHMe
H O H Me OMe N
I-274
Me OCH.sub.2 CH.sub.2 N.sub.3
H O H OMe OMe CH
I-275
Me OCH.sub.2 CH.sub.2 N.sub.3
H O H Me OMe CH
I-276
Me OCH.sub.2 CH.sub.2 N.sub.3
H O H Me OMe N
I-277
Me OCH.sub.2 OMe
H O H OMe OMe CH
I-278
Me OCH.sub.2 OMe
H O H Me OMe CH
I-279
Me OCH.sub.2 OMe
H O H Me OMe N
I-280
Me OCH.sub.2 OEt
H O H OMe OMe CH
I-281
Me OCH.sub.2 OEt
H O H Me OMe CH
I-282
Me OCH.sub.2 OEt
H O H Me OMe N
I-283
Me OCH.sub.2 OBn
H O H OMe OMe CH
I-284
Me OCH.sub.2 OBn
H O H Me OMe CH
I-285
Me OCH.sub.2 OBn
H O H Me OMe N
I-286
Me OCH.sub.2 OCH.sub.2 CF.sub.3
H O H OMe OMe CH
I-287
Me OCH.sub.2 OCH.sub.2 CF.sub.3
H O H Me OMe CH
I-288
Me OCH.sub.2 OCH.sub.2 CF.sub.3
H O H Me OMe N
I-289
Me OCH.sub.2 OBu-t
H O H OMe OMe CH
I-290
Me OCH.sub.2 OBu-t
H O H Me OMe CH
I-291
Me OCH.sub.2 OBu-t
H O H Me OMe N
I-292
Me OCH.sub.2 OCH.sub.2 CH.sub.2 OMe
H O H OMe OMe CH
I-293
Me OCH.sub.2 OCH.sub.2 CH.sub.2 OMe
H O H Me OMe CH
I-294
Me OCH.sub.2 OCH.sub.2 CH.sub.2 OMe
H O H Me OMe N
I-295
Me OCH.sub.2 CN
H O H OMe OMe CH
I-296
Me OCH.sub.2 CN
H O H Me OMe CH
I-297
Me OCH.sub.2 CN
H O H Me OMe N
I-298
Me OCH.sub.2 COOMe
H O H OMe OMe CH
I-299
Me OCH.sub.2 COOMe
H O H Me OMe CH
I-300
Me OCH.sub.2 COOMe
H O H Me OMe N
I-301
Me OCH.sub.2 COOPr
H O H OMe OMe CH
I-302
Me OCH.sub.2 COOPr
H O H Me OMe CH
I-303
Me OCH.sub.2 COOPr
H O H Me OMe N
I-304
Me OCH.sub.2 COOPr-i
H O H OMe OMe CH
I-305
Me OCH.sub.2 COOPr-i
H O H Me OMe CH
I-306
Me OCH.sub.2 COOPr-i
H O H Me OMe N
I-307
Me OCH.sub.2 SMe
H O H OMe OMe CH
I-308
Me OCH.sub.2 SMe
H O H Me OMe CH
I-309
Me OCH.sub.2 SMe
H O H Me OMe N
I-310
Me OCH.sub.2 CH.sub.2 SMe
H O H OMe OMe CH
I-311
Me OCH.sub.2 CH.sub.2 SMe
H O H Me OMe CH
I-312
Me OCH.sub.2 CH.sub.2 SMe
H O H Me OMe N
I-313
Me SCF.sub.3 H O H OMe OMe CH
I-314
Me SCF.sub.3 H O H Me OMe CH
I-315
Me SCF.sub.3 H O H Me OMe N
I-316
Me SCH.sub.2 CH.sub.2 Cl
H O H OMe OMe CH
I-317
Me SCH.sub.2 CH.sub.2 Cl
H O H Me OMe CH
I-318
Me SCH.sub.2 CH.sub.2 Cl
H O H Me OMe N
I-319
Me SCH.sub.2 CH.sub.2 F
H O H OMe OMe CH
I-320
Me SCH.sub.2 CH.sub.2 F
H O H Me OMe CH
I-321
Me SCH.sub.2 CH.sub.2 F
H O H Me OMe N
I-322
Me SOEt H O H OMe OMe CH 185-187
I-323
Me SOEt H O H Me OMe CH
I-324
Me SOEt H O H Me OMe N 136-137 (decomposed)
I-325
Me SO.sub.2 NHOEt
H O H OMe OMe CH
I-326
Me SO.sub.2 NHOEt
H O H Me OMe CH
I-327
Me SO.sub.2 NHOEt
H O H Me OMe N
I-328
Me SO.sub.2 CH.sub.2 CHCH.sub.2
H O H OMe OMe CH
I-329
Me SO.sub.2 CH.sub.2 CHCH.sub.2
H O H Me OMe CH
I-330
Me SO.sub.2 CH.sub.2 CHCH.sub.2
H O H Me OMe N
I-331
Me SO.sub.2 NEt.sub.2
H O H OMe OMe CH
I-332
Me SO.sub.2 NEt.sub.2
H O H Me OMe CH
I-333
Me SO.sub.2 NEt.sub.2
H O H Me OMe N
I-334
Me Et H O H OMe OMe CH 174-176
I-335
Me Et H O H Me OMe CH
I-336
Me Et H O H Me OMe N
I-337
Me Pr H O H OMe OMe CH 168-171
I-338
Me Pr H O H Me OMe CH
I-339
Me Pr H O H Me OMe N
I-340
Me Pr-i H O H OMe OMe CH
I-341
Me Pr-i H O H Me OMe CH
I-342
Me Pr-i H O H Me OMe N
I-343
Me Bu H O H OMe OMe CH
I-344
Me Bu H O H Me OMe CH
I-345
Me Bu H O H Me OMe N
I-346
Me Bu-t H O H OMe OMe CH
I-347
Me Bu-t H O H Me OMe CH
I-348
Me Bu-t H O H Me OMe N
I-349
Me CH.sub.2 Cl
H O H OMe OMe CH
I-350
Me CH.sub.2 Cl
H O H Me OMe CH
I-351
Me CH.sub.2 Cl
H O H Me OMe N
I-352
Me CH.sub.2 F H O H OMe OMe CH
I-353
Me CH.sub.2 F H O H Me OMe CH
I-354
Me CH.sub.2 F H O H Me OMe N
I-355
Me CH.sub.2 OMe
H O H OMe OMe CH
I-356
Me CH.sub.2 OMe
H O H Me OMe CH
I-357
Me CH.sub.2 OMe
H O H Me OMe N
I-358
Me CH.sub.2 CF.sub.3
H O H OMe OMe CH
I-359
Me CH.sub.2 CF.sub.3
H O H Me OMe CH
I-360
Me CH.sub.2 CF.sub.3
H O H Me OMe N
I-361
Me
##STR5## H O H OMe OMe CH
I-362
Me
##STR6## H O H Me OMe CH
I-363
Me
##STR7## H O H Me OMe N
I-364
Me CH.sub.2 CH.sub.2 CF.sub.3
H O H OMe OMe CH
I-365
Me CH.sub.2 CH.sub.2 CF.sub.3
H O H Me OMe CH
I-366
Me CH.sub.2 CH.sub.2 CF.sub.3
H O H Me OMe N
I-367
Me CH.sub.2 CHCH.sub.2
H O H OMe OMe CH
I-368
Me CH.sub.2 CHCH.sub.2
H O H Me OMe CH
I-369
Me CH.sub.2 CHCH.sub.2
H O H Me OMe N
I-370
Me CH.sub.2 CCH
H O H OMe OMe CH
I-371
Me CH.sub.2 CCH
H O H Me OMe CH
I-372
Me CH.sub.2 CCH
H O H Me OMe N
I-373
Me CH.sub.2 COOMe
H O H OMe OMe CH
I-374
Me CH.sub.2 COOMe
H O H Me OMe CH
I-375
Me CH.sub.2 COOMe
H O H Me OMe N
I-376
Me CH.sub.2 COOEt
H O H OMe OMe CH
I-377
Me CH.sub.2 COOEt
H O H Me OMe CH
I-378
Me CH.sub.2 COOEt
H O H Me OMe N
I-379
Me CH.sub.2 CN
H O H OMe OMe CH
I-380
Me CH.sub.2 CN
H O H Me OMe CH
I-381
Me CH.sub.2 CN
H O H Me OMe N
I-382
Me CH.sub.2 CONMe.sub.2
H O H OMe OMe CH
I-383
Me CH.sub.2 CONMe.sub.2
H O H Me OMe CH
I-384
Me CH.sub.2 CONMe.sub.2
H O H Me OMe N
I-385
Me CH.sub.2 SO.sub.2 NMe.sub.2
H O H OMe OMe CH
I-386
Me CH.sub.2 SO.sub.2 NMe.sub.2
H O H Me OMe CH
I-387
Me CH.sub.2 SO.sub.2 NMe.sub.2
H O H Me OMe N
I-388
Me CH.sub.2 NMe.sub.2
H O H OMe OMe CH
I-389
Me CH.sub.2 NMe.sub.2
H O H Me OMe CH
I-390
Me CH.sub.2 NMe.sub.2
H O H Me OMe N
I-391
Me CHCH.sub.2 H O H OMe OMe CH
I-392
Me CHCH.sub.2 H O H Me OMe CH
I-393
Me CHCH.sub.2 H O H Me OMe N
I-394
Me CHCHMe H O H OMe OMe CH
I-395
Me CHCHMe H O H Me OMe CH
I-396
Me CHCHMe H O H Me OMe N
I-397
Me CCH H O H OMe OMe CH
I-398
Me CCH H O H Me OMe CH
I-399
Me CCH H O H Me OMe N
I-400
Me CCMe H O H OMe OMe CH
I-401
Me CCMe H O H Me OMe CH
I-402
Me CCMe H O H Me OMe N
I-403
Me CHCHCOOMe H O H OMe OMe CH
I-404
Me CHCHCOOMe H O H Me OMe CH
I-405
Me CHCHCOOMe H O H Me OMe N
I-406
Me CH(Me)COMe H O H OMe OMe CH
I-407
Me CH(Me)COMe H O H Me OMe CH
I-408
Me CH(Me)COMe H O H Me OMe N
I-409
Me CH(Me)COEt H O H OMe OMe CH
I-410
Me CH(Me)COEt H O H Me OMe CH
I-411
Me CH(Me)COEt H O H Me OMe N
I-412
Me CH(Et)COMe H O H OMe OMe CH
I-413
Me CH(Et)COMe H O H Me OMe CH
I-414
Me CH(Et)COMe H O H Me OMe N
I-415
Me CH(Et)COEt H O H OMe OMe CH
I-416
Me CH(Et)COEt H O H Me OMe CH
I-417
Me CH(Et)COEt H O H Me OMe N
I-418
Me
##STR8## H O H OMe OMe CH
I-419
Me
##STR9## H O H Me OMe CH
I-420
Me
##STR10## H O H Me OMe N
I-421
Me COPr H O H OMe OMe CH
I-422
Me COPr H O H Me OMe CH
I-423
Me COPr H O H Me OMe N
I-424
Me COPr-i H O H OMe OMe CH
I-425
Me COPr-i H O H Me OMe CH
I-426
Me COPr-i H O H Me OMe N
I-427
Me CHNOMe H O H OMe OMe CH
I-428
Me CHNOMe H O H Me OMe CH
I-429
Me CHNOMe H O H Me OMe N
I-430
Me CHNOEt H O H OMe OMe CH
I-431
Me CHNOEt H O H Me OMe CH
I-432
Me CHNOEt H O H Me OMe N
I-433
Me C(Me)NOMe H O H OMe OMe CH
I-434
Me C(Me)NOMe H O H Me OMe CH
I-435
Me C(Me)NOMe H O H Me OMe N
I-436
Me C(Me)NOEt H O H OMe OMe CH
I-437
Me C(Me)NOEt H O H Me OMe CH
I-438
Me C(Me)NOEt H O H Me OMe N
I-439
Me C(Me)NOPr H O H OMe OMe CH
I-440
Me C(Me)NOPr H O H Me OMe CH
I-441
Me C(Me)NOPr H O H Me OMe N
I-442
Me C(Me)NOCH.sub.2 CH.sub.2 Cl
H O H OMe OMe CH
I-443
Me C(Me)NOCH.sub.2 CH.sub.2 Cl
H O H Me OMe CH
I-444
Me C(Me)NOCH.sub.2 CH.sub.2 Cl
H O H Me OMe N
I-445
Me C(Me)NOCH.sub.2 CH.sub.2 F
H O H OMe OMe CH
I-446
Me C(Me)NOCH.sub.2 CH.sub.2 F
H O H Me OMe CH
I-447
Me C(Me)NOCH.sub.2 CH.sub.2 F
H O H Me OMe N
I-448
Me NHEt H O H OMe OMe CH
I-449
Me NHEt H O H Me OMe CH
I-450
Me NHEt H O H Me OMe N
I-451
Me NHPr H O H OMe OMe CH
I-452
Me NHPr H O H Me OMe CH
I-453
Me NHPr H O H Me OMe N
I-454
Me NHCOOMe H O H OMe OMe CH
I-455
Me NHCOOMe H O H Me OMe CH
I-456
Me NHCOOMe H O H Me OMe N
I-457
Me NHCOOEt H O H OMe OMe CH
I-458
Me NHCOOEt H O H Me OMe CH
I-459
Me NHCOOEt H O H Me OMe N
I-460
Me NHCOOPh H O H OMe OMe CH
I-461
Me NHCOOPh H O H Me OMe CH
I-462
Me NHCOOPh H O H Me OMe N
I-463
Me N(Me)SO.sub.2 Me
H O H OMe OMe CH
I-464
Me N(Me)SO.sub.2 Me
H O H Me OMe CH
I-465
Me N(Me)SO.sub.2 Me
H O H Me OMe N
I-466
Me N(Et)SO.sub.2 Me
H O H OMe OMe CH
I-467
Me N(Et)SO.sub.2 Me
H O H Me OMe CH
I-468
Me N(Et)SO.sub.2 Me
H O H Me OMe N
I-469
Me N(Me)SO.sub.2 Et
H O H OMe OMe CH
I-470
Me N(Me)SO.sub.2 Et
H O H Me OMe CH
I-471
Me N(Me)SO.sub.2 Et
H O H OMe OMe N
I-472
Me N(Et)SO.sub.2 Et
H O H OMe OMe CH
I-473
Me N(Et)SO.sub.2 Et
H O H Me OMe CH
I-474
Me N(Et)SO.sub.2 Et
H O H Me OMe N
I-475
Me NHCOEt H O H OMe OMe CH
I-476
Me NHCOEt H O H Me OMe CH
I-477
Me NHCOEt H O H Me OMe N
I-478
Me NHCOCF.sub.3
H O H OMe OMe CH
I-479
Me NHCOCF.sub.3
H O H Me OMe CH
I-480
Me NHCOCF.sub.3
H O H Me OMe N
I-481
Me NCHMe H O H OMe OMe CH
I-482
Me NCHMe H O H Me OMe CH
I-483
Me NCHMe H O H Me OMe N
I-484
Me NCHPh H O H OMe OMe CH
I-485
Me NCHPh H O H Me OMe CH
I-486
Me NCHPh H O H Me OMe N
I-487
Me N.sub.3 H O H OMe OMe CH
I-488
Me N.sub.3 H O H Me OMe CH
I-489
Me N.sub.3 H O H Me OMe N
I-490
Me I H O H OMe OMe CH
I-491
Me I H O H Me OMe CH
I-492
Me I H O H Me OMe N
I-493
Me OCOEt H O H OMe OMe CH
I-494
Me OCOEt H O H Me OMe CH
I-495
Me OCOEt H O H Me OMe N
I-496
Me OCOPr H O H OMe OMe CH
I-497
Me OCOPr H O H Me OMe CH
I-498
Me OCOPr H O H Me OMe N
I-499
Me OCOPh H O H OMe OMe CH
I-500
Me OCOPh H O H Me OMe CH
I-501
Me OCOPh H O H Me OMe N
I-502
Me OCONMe.sub.2
H O H OMe OMe CH
I-503
Me OCONMe.sub.2
H O W Me OMe CH
I-504
Me OCONMe.sub.2
H O H Me OMe N
I-505
Me Cl H O H CF.sub.3
OMe CH
I-506
Me OPr-i H O H Cl OMe CH 163-165
I-507
Me SEt H O H Me OMe CH 225-227
I-508
Me SEt H O H Cl OMe CH 185-187
I-509
Me SEt H O H Me Me CH 220-222
I-510
Me SEt H O H OMe OMe N 173-175
I-511
Me SBu H O H OMe Me CH 157-160
I-512
Me SBu H O H OMe Me N 155-157
I-513
Me SPr-i H O H OMe Me CH 185-187
I-514
Me SPr-i H O H OMe Me N 228-229
I-515
Me SOEt H O H OMe OMe N 180-182
I-516
Me SO.sub.2 Et
H O H OMe Me CH 270-272
I-517
Me SO.sub.2 Et
H O H OMe Me N 165-168
I-518
Me SO.sub.2 Et
H O H OMe Cl CH 272-275
I-519
Me SO.sub.2 Pr
H O H OMe Me CH 265-267
I-520
Me SO.sub.2 Pr
H O H OMe Me N 132-135
I-521
Me SO.sub.2 Pr
H O H OMe Cl CH 142-145
I-522
Me SO.sub.2 Bu
H O H OMe Me CH 243-246
I-523
Me SO.sub.2 Bu
H O H OMe Me N 241-243
I-524
Me SO.sub.2 Bu
H O H OMe Cl CH 245-247
I-525
Me SO.sub.2 Pr-i
H O H OMe Me CH 135-139
I-526
Me SO.sub.2 Pr-i
H O H OMe Me N 281-282
I-527
Me COOPr H O H OMe Me N 187-189
I-528
Me NO.sub.2 H O H OMe Cl CH 204-206
I-529
Me CONMe.sub.2
H O H OMe Me CH 161-164
I-530
Me Br H O H OMe Cl CH 276-279
I-531
Me
##STR11## H O H OMe OMe CH
I-532
Me OCH.sub.2Bu-t
H O H OMe OMe CH
I-533
Me OCH.sub.2Bu-t
H O H Me OMe CH
I-534
Me OCH.sub.2 CHCMe.sub.2
H O H OMe OMe CH
I-535
Me OCH.sub.2 CH.sub.2 CH.sub.2 F
H O H OMe OMe CH
I-536
Me OCH.sub.2 CH.sub.2 CH.sub.2 F
H O H Me OMe CH
I-537
Me OCH.sub.2 CH.sub.2 CH.sub.2 F
H O H Me OMe N
I-538
Me CH.sub.2 CH.sub.2 N.sub.3
H O H OMe OMe CH
I-539
Me
##STR12## H O H OMe OMe CH
I-540
Me COCF.sub.3 H O H OMe OMe CH
I-541
Me COOCH.sub.2 CHCHCl
H O H OMe OMe CH
I-542
Me SO.sub.2 CF.sub.3
H O H OMe OMe CH
I-543
Me OCOCF.sub.3
H O H OMe OMe CH
I-544
Me OCH.sub.2 OPh
H O H OMe OMe CH
I-545
Me CHNOH H O H OMe OMe CH
I-546
Me CHNOCH.sub.2 CHCH.sub.2
H O H OMe OMe CH
I-547
Me CHNOCH.sub.2 CCH
H O H OMe OMe CH
I-548
Me C(Me)NOBn H O H OMe OMe CH
I-549
Me C(Me)NOPh H O H OMe OMe CH
I-550
Me C(Bn)NOMe H O H OMe OMe CH
I-551
Me C(Ph)NOMe H O H OMe OMe CH
I-552
Me C(CF.sub.3)NOMe
H O H OMe OMe CH
I-553
Me COOCH.sub.2 CH.sub.2 Cl
H O H OMe OMe CH
I-554
Me COOCH.sub.2 CF.sub.3
H O H OMe OMe CH
I-555
Me Cl 5-Cl O H OMe Me N 182-184
I-556
Me Cl 5-OMe O H OMe OMe CH
I-557
Me Cl 5-F O H OMe OMe CH
I-558
Me F 5-Cl O H OMe OMe CH
I-559
Me F 5-F O H OMe OMe CH
I-560
Me COOMe 5-Cl O H OMe OMe CH
I-561
Me COOEt 5-Cl O H OMe OMe CH
I-562
Me COOPr 5-Cl O H OMe OMe CH
I-563
Me COOPr-i 5-Cl O H OMe OMe CH
I-564
Me OMe 5-COOMe O H OMe OMe CH
I-565
Me COOMe 5-OMe O H OMe OMe CH
I-566
Me H 5-CN O H OMe OMe CH
I-567
Me H 5-CF.sub.3
O H OMe OMe CH
I-568
Me H 5-COOMe O H OMe OMe CH 235-236
I-569
Me H 5-COOEt O H OMe OMe CH
I-570
Me H 5-COOPr O H OMe OMe CH
I-571
Me H 5-COOPr-i
O H OMe OMe CH
I-572
Me H 5-COOCH.sub.2 CH.sub.2 Cl
O H OMe OMe CH
I-573
Me H 5-COOCH.sub.2 CH.sub.2 F
O H OMe OMe CH
I-574
Me H 5-COOCH.sub.2 CF.sub.3
O H OMe OMe CH
I-575
Me H 5-COOCH.sub.2 OMe
O H OMe OMe CH
I-576
Me H 5-CONMe.sub.2
O H OMe OMe CH
I-577
Me H 5-OCH.sub.2 CH.sub.2 F
O H OMe OMe CH
I-578
Me H 5-OCHF.sub.2
O H OMe OMe CH
I-579
Me H 5-OCH.sub.2 CF.sub.3
O H OMe OMe CH
I-580
Me H 5-OCH.sub.2 CH.sub.2 CH.sub.2 F
O H OMe OMe CH
I-581
Me H 5-OCH.sub.2 CHCH.sub.2
O H OMe OMe CH
I-582
Me H 5-OCH.sub.2 CCH
O H OMe OMe CH
I-583
Me H 5-NO.sub.2
O H OMe OMe CH
I-584
Me H 5-SMe O H OMe OMe CH
I-585
Me H 5-SEt O H OMe OMe CH
I-586
Me H 5-SPr O H OMe OMe CH
I-587
Me H 5-SPr-i O H OMe OMe CH
I-588
Me H 5-SO.sub.2 Et
O H OMe OMe CH
I-589
Me H 5-SO.sub.2 Pr
O H OMe OMe CH
I-590
Me H 5-SO.sub.2 Pr-i
O H OMe OMe CH
I-591
Me H 5-SOEt O H OMe OMe CH
I-592
Me H 5-Me O H OMe OMe CH
I-593
Me H 5-Et O H OMe OMe CH
I-594
Me H 5-Pr O H OMe OMe CH
I-595
Me H 5-SO.sub.2 NMe.sub.2
O H OMe OMe CH
I-596
Me H 5-OCF.sub.3
O H OMe OMe CH
I-597
Me H 5-CH.sub.2 CF.sub.3
O H OMe OMe CH
I-598
Me H 5-CH.sub.2 CHCH.sub.2
O H OMe OMe CH
I-599
Me H 5-COOMe O H OMe Me CH 134-135
I-600
Me H 5-COOMe O H OMe Me N 143-144
I-601
Me H 5-COOMe O H OMe OMe N 148-150
I-602
Me
##STR13## H O H OMe OMe CH
I-603
Me
##STR14## H O H Me OMe CH
I-604
Me
##STR15## H O H Me OMe N
I-605
Me
##STR16## H O H OMe OMe CH
I-606
Me
##STR17## H O H Me OMe CH
I-607
Me
##STR18## H O H Me OMe N
I-608
Me
##STR19## H O H OMe OMe CH
I-609
Me
##STR20## H O H Me OMe CH
I-610
Me
##STR21## H O H Me OMe N
I-611
Me OC.sub.2 H.sub.4O* O H OMe OMe CH
I-612
Me OC.sub.2 H.sub.4O* O H Me OMe CH
I-613
Me OC.sub.2 H.sub.4O* O H Me OMe N
I-614
Me SC.sub.2 H.sub.4S* O H OMe OMe CH
I-615
Me SC.sub.2 H.sub.4S* O H Me OMe CH
I-616
Me SC.sub.2 H.sub.4S* O H Me OMe N
I-617
Me OCH.sub.2O* O H OMe OMe CH
I-618
##STR22##
Cl H O H OMe OMe CH
I-619
##STR23##
Cl H O H OMe OMe CH
I-620
##STR24##
Cl H O H OMe OMe CH
I-621
COMe Cl H O H OMe OMe CH
I-622
COEt Cl H O H OMe OMe CH
I-623
COPr Cl H O H OMe OMe CH
I-624
COPr-i Cl H O H OMe OMe CH
I-625
COPh Cl H O H OMe OMe CH
I-626
SO.sub.2 Me
Cl H O H OMe OMe CH
I-627
SO.sub.2 Et
Cl H O H OMe OMe CH
I-628
SO.sub.2 Ph
Cl H O H OMe OMe CH
I-629
COOMe Cl H O H OMe OMe CH
I-630
COOEt Cl H O H OMe OMe CH
I-631
COOPh Cl H O H OMe OMe CH
I-632
CONMe.sub.2
Cl H O H OMe OMe CH
I-633
SO.sub.2 NMe.sub.2
Cl H O H OMe OMe CH
I-634
Ph Cl H O H Me OMe N
I-635
CH.sub.2 OMe
Cl H O H OMe OMe CH
I-636
CH.sub.2 OBn
Cl H O H OMe OMe CH
I-637
CH.sub.2 CH.sub.2 F
Cl H O H OMe OMe CH
I-638
CH.sub.2 CH.sub.2 Cl
Cl H O H OMe OMe CH
I-639
CF.sub.3
Cl H O H OMe OMe CH
I-640
CH.sub.2 F
Cl H O H OMe OMe CH
I-641
CH.sub.2 CHCH.sub.2
OMe H O H OMe OMe CH 221-223
I-642
COCF.sub.3
Cl H O H OMe OMe CH
I-643
##STR25##
Cl H O H OMe OMe CH
I-644
H Bn H O H OMe OMe CH
I-645
H Br H O H OMe Me CH 183-184
I-646
H Br H O H OMe Me N 154-155
I-647
H Br H O H OMe OMe CH
I-648
H Bu H O H Me OMe CH
I-649
H Bu H O H Me OMe N
I-650
H Bu H O H OMe OMe CH
I-651
H Bu-t H O H Me OMe CH
I-652
H Bu-t H O H Me OMe N
I-653
H Bu-t H O H OMe OMe CH
I-654
H C(Me)NOCH.sub.2 CH.sub.2 Cl
H O H Me OMe CH
I-655
H C(Me)NOCH.sub.2 CH.sub.2 Cl
H O H Me OMe N
I-656
H C(Me)NOCH.sub.2 CH.sub.2 Cl
H O H OMe OMe CH
I-657
H C(Me)NOCH.sub.2 CH.sub.2 F
H O H Me OMe CH
I-658
H C(Me)NOCH.sub.2 CH.sub.2 F
H O H Me OMe N
I-659
H C(Me)NOCH.sub.2 CH.sub.2 F
H O H OMe OMe CH
I-660
H C(Me)NOEt H O H Me OMe CH
I-661
H C(Me)NOEt H O H Me OMe N
I-662
H C(Me)NOEt H O H OMe OMe CH
I-663
H C(Me)NOMe H O H Me OMe CH
I-664
H C(Me)NOMe H O H Me OMe N
I-665
H C(Me)NOMe H O H OMe OMe CH
I-666
H C(Me)NOPr H O H Me OMe CH
I-667
H C(Me)NOPr H O H Me OMe N
I-668
H C(Me)NOPr H O H OMe OMe CH
I-669
H CCH H O H Me OMe CH
I-670
H CCH H O H Me OMe N
I-671
H CCH H O H OMe OMe CH
I-672
H CCMe H O H Me OMe CH
I-673
H CCMe H O H Me OMe N
I-674
H CCMe H O H OMe OMe CH
I-675
H CF.sub.3 H O H OMe OMe CH
I-676
H CH(Et)COEt H O H Me OMe CH
I-677
H CH(Et)COEt H O H Me OMe N
I-678
H CH(Et)COEt H O H OMe OMe CH
I-679
H CH(Et)COMe H O H Me OMe CH
I-680
H CH(Et)COMe H O H Me OMe N
I-681
H CH(Et)COMe H O H OMe OMe CH
I-682
H CH(Me)COEt H O H Me OMe CH
I-683
H CH(Me)COEt H O H Me OMe N
I-684
H CH(Me)COEt H O H OMe OMe CH
I-685
H CH(Me)COMe H O H Me OMe CH
I-686
H CH(Me)COMe H O H Me OMe N
I-687
H CH(Me)COMe H O H OMe OMe CH
I-688
H CHCHCOOMe H O H Me OMe CH
I-689
H CHCHCOOMe H O H Me OMe N
I-690
H CHCHCOOMe H O H OMe OMe CH
I-691
H CHCH.sub.2 H O H Me OMe CH
I-692
H CHCH.sub.2 H O H Me OMe N
I-693
H CHCH.sub.2 H O H OMe OMe CH
I-694
H CHCHMe H O H Me OMe CH
I-695
H CHCHMe H O H Me OMe N
I-696
H CHCHMe H O H OMe OMe CH
I-697
H CHNOEt H O H Me OMe CH
I-698
H CHNOEt H O H Me OMe N
I-699
H CHNOEt H O H OMe OMe CH
I-700
H CHNOMe H O H Me OMe CH
I-701
H CHNOMe H O H Me OMe N
I-702
H CHNOMe H O H OMe OMe CH
I-703
H CH.sub.2 CCH
H O H Me OMe CH
I-704
H CH.sub.2 CCH
H O H Me OMe N
I-705
H CH.sub.2 CCH
H O H OMe OMe CH
I-706
H CH.sub.2 CF.sub.3
H O H Me OMe CH
I-707
H CH.sub.2 CF.sub.3
H O H Me OMe N
I-708
H CH.sub.2 CF.sub.3
H O H OMe OMe CH
I-709
H CH.sub.2 CHCH.sub.2
H O H Me OMe CH
I-710
H CH.sub.2 CHCH.sub.2
H O H Me OMe N
I-711
H CH.sub.2 CHCH.sub.2
H O H OMe OMe CH
I-712
H CH.sub.2 CH.sub.2 CF.sub.3
H O H Me OMe CH
I-713
H CH.sub.2 CH.sub.2 CF.sub.3
H O H Me OMe N
I-714
W CH.sub.2 CH.sub.2 CF.sub.3
H O H OMe OMe CH
I-715
H CH.sub.2 CN
H O H Me OMe CH
I-716
H CH.sub.2 CN
H O H Me OMe N
I-717
H CH.sub.2 CN
H O H OMe OMe CH
I-718
H CH.sub.2 CONMe.sub.2
H O H Me OMe CH
I-719
H CH.sub.2 CONMe.sub.2
H O H Me OMe N
I-720
H CH.sub.2 CONMe.sub.2
H O H OMe OMe CH
I-721
H CH.sub.2 COOEt
H O H Me OMe CH
I-722
H CH.sub.2 COOEt
H O H Me OMe N
I-723
H CH.sub.2 COOEt
H O H OMe OMe CH
I-724
H CH.sub.2 COOMe
H O H Me OMe CH
I-725
H CH.sub.2 COOMe
H O H Me OMe N
I-726
H CH.sub.2 COOMe
H O H OMe OMe CH
I-727
H CH.sub.2 Cl
H O H Me OMe CH
I-728
H CH.sub.2 Cl
H O H Me OMe N
I-729
H CH.sub.2 Cl
H O H OMe OMe CH
I-730
H CH.sub.2 F H O H Me OMe CH
I-731
H CH.sub.2 F H O H Me OMe N
I-732
H CH.sub.2 F H O H OMe OMe CH
I-733
H CH.sub.2 NMe.sub.2
H O H Me OMe CH
I-734
H CH.sub.2 NMe.sub.2
H O H Me OMe N
I-735
H CH.sub.2 NMe.sub.2
H O H OMe OMe CH
I-736
H CH.sub.2 OMe
H O H Me OMe CH
I-737
H CH.sub.2 OMe
H O H Me OMe N
I-738
H CH.sub.2 OMe
H O H OMe OMe CH
I-739
H CH.sub.2 SO.sub.2 NMe.sub.2
H O H Me OMe CH
I-740
H CH.sub.2 SO.sub.2 NMe.sub.2
H O H Me OMe N
I-741
H CH.sub.2 SO.sub.2 NMe.sub.2
H O H OMe OMe CH
I-742
H CN H O H OMe Me CH
I-743
H CN H O H OMe Me N
I-744
H CN H O H OMe OMe CH
I-745
H
##STR26## H O H Me OMe CH
I-746
H
##STR27## H O H Me OMe N
I-747
H
##STR28## H O H OMe OMe CH
I-748
H CO.sub.2 Bn
H O H OMe OMe CH
I-749
H CO.sub.2 Bu
H O H OMe Me CH
I-750
H CO.sub.2 Bu
H O H OMe Me N
I-751
H CO.sub.2 Bu
H O H OMe OMe CH
I-752
H CO.sub.2 CH.sub.2 CCH
H O H OMe OMe CH
I-753
H CO.sub.2 CH.sub.2 CHCH.sub.2
H O H OMe OMe CH
I-754
H CO.sub.2 CH.sub.2 CH.sub.2 F
H O H OMe OMe CH
I-755
H CO.sub.2 Et
H O H OCHF.sub.2
OCHF.sub.2
CH
I-756
H CO.sub.2 Et
H O H OMe Me N
I-757
H CO.sub.2 Et
H S H OMe OMe CH
I-758
H CO.sub.2 H H O H OMe OMe CH
I-759
H CO.sub.2 Me
5-F O H OMe OMe CH
I-760
H CO.sub.2 Me
H O H OCHF.sub.2
OCHF.sub.2
CH
I-761
H CO.sub.2 Me
H O H OMe Me CH 202-205
I-762
H CO.sub.2 Me
H O H OMe Me N 169-170
I-763
H CO.sub.2 Me
H O H OMe OCHF.sub.2
CH
I-764
H CO.sub.2 Me
H O Me OMe OMe CH
I-765
H CO.sub.2 Me
H S H OMe OMe CH
I-766
H CO.sub.2 Pen
H O H OMe OMe CH
I-767
H CO.sub.2 Ph
H O H OMe OMe CH
I-768
H CO.sub.2 Pr
H O H OMe Me CH
I-769
H CO.sub.2 Pr
H O H OMe OMe CH
I-770
H CO.sub.2 Pr-i
H O H OMe Me CH
I-771
H CO.sub.2 Pr-i
H O H OMe Me N
I-772
H CO.sub.2 Pr-i
H O H OMe OMe CH
I-773
H COBn H O H OMe OMe CH
I-774
H COCH.sub.2 CCH
H O H OMe OMe CH
I-775
H COCH.sub.2 CHCH.sub.2
H O H OMe OMe CH
I-776
H COEt H O H OMe OMe CH
I-777
H COH H O H OMe OMe CH
I-778
H COMe H O H OMe OMe CH
I-779
H CON(Et).sub.2
H O H OMe OMe CH
I-780
H CON(Me).sub.2
H O H OMe OMe CH
I-781
H CONH.sub.2 H O H OMe OMe CH
I-782
H CONHBn H O H OMe OMe CH
I-783
H CONHCH.sub.2 CCH
H O H OMe OMe CH
I-784
H CONHCH.sub.2 CHCH.sub.2
H O H OMe OMe CH
I-785
H CONHEt H O H OMe OMe CH
I-786
H CONHMe H O H OMe OMe CH
I-787
H CONHOMe H O H OMe OMe CH
I-788
H CONHPh H O H OMe OMe CH
I-789
H CONHPr H O H OMe OMe CH
I-790
H COOMe H O H OMe Me CH
I-791
H COOMe H O H Me OMe N
I-792
H COPh H O H OMe OMe CH
I-793
H COPr H O H Me OMe CH
I-794
H COPr H O H Me OMe N
I-795
H COPr H O H OMe OMe CH
I-796
H COPr-i H O H Me OMe CH
I-797
H COPr-i H O H Me OMe N
I-798
H COPr-i H O H OMe OMe CH
I-799
H Cl 5-Cl O H OMe OMe CH
I-800
H Cl H S H Cl OMe CH
I-801
H Cl H O H Me Me CH
I-802
H Cl H O H OMe Me CH
I-803
H Cl H O H OMe Me N
I-804
H Cl H S H Me Me CH
I-805
H Cl H S H OMe Me CH
I-806
H Cl H S H OMe Me N
I-807
H Cl H O Me OMe OMe CH
I-808
H Cl H S H OMe OMe CH
I-809
H Et H O H Me OMe CH
I-810
H Et H O H Me OMe N
I-811
H Et H O H OMe OMe CH
I-812
H F H O H Me Me CH
I-813
H F H O H OMe Me CH
I-814
H F H O H OMe Me N
I-815
H F H O H OMe OMe CH
I-816
H H 5-Cl O H Me Me CH
I-817
H H 5-Cl O H OMe Me N
I-818
H H 5-Cl O H OMe OMe CH
I-819
H H 5-F O H Me Me CH
I-820
H H 5-F O H OMe Me CH
I-821
H H 5-F O H OMe Me N
I-822
H H 5-F O H OMe OMe CH
I-823
H H 5-OEt O H OMe Me CH
I-824
H H 5-OEt O H OMe Me N
I-825
H H 5-OEt O H OMe OMe CH
I-826
H H 5-OEt O H OMe OMe N
I-827
H H 5-OMe O H Cl OMe CH
I-828
H H 5-OMe O H OMe Me CH
I-829
H H 5-OMe O H OMe Me N
I-830
H H 5-OMe O H OMe OMe CH
I-831
H H 5-OPr O H OMe Me CH
I-832
H H 5-OPr O H OMe Me N
I-833
H H 5-OPr O H OMe OMe CH
I-834
H H 5-OPr O H OMe OMe N
I-835
H H 6-Cl O H Me Me CH
I-836
H H 6-Cl O H OMe Me N
I-837
H H 6-Cl O H OMe OMe CH
I-838
H H 7-Cl O H OMe Me N
I-839
H H 7-Cl O H OMe OMe CH
I-840
H H H O H Me Me CH
I-841
H H H O H OMe Me N
I-842
H H H O H OMe OMe CH
I-843
H I H O H Me OMe CH
I-844
H I H O H Me OMe N
I-845
H I H O H OMe OMe CH
I-846
H Me H O H OMe OMe CH
I-847
H N(Et)SO.sub.2 Et
H O H Me OMe CH
I-848
H N(Et)SO.sub.2 Et
H O H Me OMe N
I-849
H N(Et)SO.sub.2 Et
H O H OMe OMe CH
I-850
H N(Et)SO.sub.2 Me
H O H Me OMe CH
I-851
H N(Et)SO.sub.2 Me
H O H Me OMe N
I-852
H N(Et)SO.sub.2 Me
H O H OMe OMe CH
I-853
H N(Me).sub.2
H O H OMe OMe CH
I-854
H N(Me)SO.sub.2 Et
H O H Me OMe CH
I-855
H N(Me)SO.sub.2 Et
H O H Me OMe N
I-856
H N(Me)SO.sub.2 Et
H O H OMe OMe CH
I-857
H N(Me)SO.sub.2 Me
H O H Me OMe CH
I-858
H N(Me)SO.sub.2 Me
H O H Me OMe N
I-859
H N(Me)SO.sub.2 Me
H O H OMe OMe CH
I-860
H NCHPh H O H Me OMe CH
I-861
H NCHPh H O H Me OMe N
I-862
H NCHPh H O H OMe OMe CH
I-863
H NCHMe H O H Me OMe CH
I-864
H NCHMe H O H Me OMe N
I-865
N NCHMe H O H OMe OMe CH
I-866
H N.sub.3 H O H Me OMe CH
I-867
H N.sub.3 H O H Me OMe N
I-868
H N.sub.3 H O H OMe OMe CH
I-869
H NEt.sub.2 H O H OMe OMe CH
I-870
H NH.sub.2 H O H OMe OMe CH
I-871
H NHBn H O H Cl OMe CH
I-872
H NHBn H O H OMe OMe CH
I-873
H NHCOCF.sub.3
H O H Me OMe CH
I-874
H NHCOCF.sub.3
H O H Me OMe N
I-875
H NHCOCF.sub.3
H O H OMe OMe CH
I-876
H NHCOCH.sub.2 Cl
H O H OMe OMe CH
I-877
H NHCOEt H O H Me OMe CH
I-878
H NHCOEt H O H Me OMe N
I-879
H NHCOEt H O H OMe OMe CH
I-880
H NHCOMe H O H OMe OMe CH
I-881
H NHCOOEt H O H Me OMe CH
I-882
H NHCOOEt H O H Me OMe N
I-883
H NHCOOEt H O H OMe OMe CH
I-884
H NHCOOMe H O H Me OMe CH
I-885
H NHCOOMe H O H Me OMe N
I-886
H NHCOOMe H O H OMe OMe CH
I-887
H NHCOOPh H O H Me OMe CH
I-888
H NHCOOPh H O H Me OMe N
I-889
H NHCOOPh H O H OMe OMe CH
I-890
H NHCOPh H O H OMe OMe CH
I-891
H NHEt H O H Me OMe CH
I-892
H NHEt H O H Me OMe N
I-893
H NHEt H O H OMe OMe CH
I-894
N NHMe H O H OMe Me CH
I-895
H NHMe H O H OMe Me N
I-896
H NHMe H O H OMe OMe CH
I-897
H NHPr H O H Me OMe CH
I-898
H NHPr H O H Me OMe N
I-899
H NHPr H O H OMe OMe CH
I-900
H NHSO.sub.2 CH.sub.3
H O H OMe OMe CH
I-901
H NHSO.sub.2 Ph
H O H OMe OMe CH
I-902
H NMe.sub.2 H O H Cl OMe CH
I-903
H NMe.sub.2 H O H Me Me CH
I-904
H NMe.sub.2 H O H OMe Me N
I-905
H NO.sub.2 H O H OMe Me CH 208-210
I-906
H NO.sub.2 H O H OMe OMe CH 184-186
I-907
H OBn H O H OMe OMe CH
I-908
H OBn(2-Me) H O H OMe OMe CH
I-909
H OBn(3-OMe) H O H OMe OMe CH
I-910
H OBn(4-Cl) H O H OMe OMe CH
I-911
H OBu H O H Cl OMe CH
I-912
H OBu H O H Me Me CH
I-913
H OBu H O H OMe Me CH
I-914
H OBu H O H OMe Me N
I-915
H OBu H O H OMe OMe CH
I-916
H OCF.sub.2 CH.sub.2 Cl
H O H Me OMe CH
I-917
H OCF.sub.2 CH.sub.2 Cl
H O H Me OMe N
I-918
H OCF.sub.2 CH.sub.2 Cl
H O H OMe OMe CH
I-919
H OCF.sub.2 CHFCl
H O H Me OMe CH
I-920
H OCF.sub.2 CHFCl
H O H Me OMe N
I-921
H OCF.sub.2 CHFCl
H O H OMe OMe CH
I-922
H OCF.sub.3 H O H Me OMe CH
I-923
H OCF.sub.3 H O H Me OMe N
I-924
H OCF.sub.3 H O H OMe OMe CH
I-925
H OCH(CF.sub.2 CF.sub.3)Me
H O H Me OMe CH
I-926
H OCH(CF.sub.2 CF.sub.3)Me
H O H Me OMe N
I-927
H OCH(CF.sub.2 CF.sub.3)Me
H O H OMe OMe CH
I-928
H OCH(CF.sub.3)Me
H O H OMe Me CH
I-929
H OCH(CF.sub.3)Me
H O H OMe OMe CH
I-930
H OCH.sub.2 C(Cl)CH.sub.2
H O H Me OMe CH
I-931
H OCH.sub.2 C(Cl)CH.sub.2
H O H Me OMe N
I-932
H OCH.sub.2 C(Cl)CH.sub.2
H O H OMe OMe CH
I-933
H OCH.sub.2 C(Me)CH.sub.2
H O H Me OMe CH
I-934
H OCH.sub.2 C(Me)CH.sub.2
H O H Me OMe N
I-935
H OCH.sub.2 C(Me)CH.sub.2
H O H OMe OMe CH
I-936
H OCH.sub.2 CCH
H O H OMe OMe CH
I-937
H OCH.sub.2 CF.sub.2 CF.sub.3
H O H Me OMe CH
I-938
H OCH.sub.2 CF.sub.2 CF.sub.3
H O H Me OMe N
I-939
H OCH.sub.2 CF.sub.2 CF.sub.3
H O H OMe OMe CH
I-940
H OCH.sub.2 CF.sub.2 CHF.sub.2
H O H Me OMe CH
I-941
H OCH.sub.2 CF.sub.2 CHF.sub.2
H O H Me OMe N
I-942
H OCH.sub.2 CF.sub.2 CHF.sub.2
H O H OMe OMe CH
I-943
H OCH.sub.2 CF.sub.3
H O H Cl OMe CH
I-944
H OCH.sub.2 CF.sub.3
H O H OMe Me CH
I-945
H OCH.sub.2 CF.sub.3
H O H OMe Me N
I-946
H OCH.sub.2 CF.sub.3
H O H OMe OMe CH
I-947
H OCH.sub.2 CHCCl.sub.2
H O H Me OMe CH
I-948
H OCH.sub.2 CHCCl.sub.2
H O H Me OMe N
I-949
H OCH.sub.2 CHCCl.sub.2
H O H OMe OMe CH
I-950
H OCH.sub.2 CHCHCl
H O H Me OMe CH
I-951
H OCH.sub.2 CHCHCl
H O H Me OMe N
I-952
H OCH.sub.2 CHCHCl
H O H OMe OMe CH
I-953
H OCH.sub.2 CHCH.sub.2
H O H OMe OMe CH
I-954
H OCH.sub.2 CHCHMe
H O H Me OMe CH
I-955
H OCH.sub.2 CHCHMe
H O H Me OMe N
I-956
H OCH.sub.2 CHCHMe
H O H OMe OMe CH
I-957
H OCH.sub.2 CH.sub.2 CF.sub.3
H O H Me OMe CH
I-958
H OCH.sub.2 CH.sub.2 CF.sub.3
H O H Me OMe N
I-959
H OCH.sub.2 CH.sub.2 CF.sub.3
H O H OMe OMe CH
I-960
H OCH.sub.2 CH.sub.2 Cl
H O H OMe OMe CH
I-961
H OCH.sub.2 CH.sub.2 F
H O H OMe OMe CH
I-962
H OCH.sub.2 CH.sub.2 N.sub.3
H O H Me OMe CH
I-963
H OCH.sub.2 CH.sub.2 N.sub.3
H O H Me OMe N
I-964
H OCH.sub.2 CH.sub.2 N.sub.3
H O H OMe OMe CH
I-965
H OCH.sub.2 CH.sub.2 NMe.sub.2
H O H OMe Me CH
I-966
H OCH.sub.2 CH.sub.2 NMe.sub.2
H O H OMe Me N
I-967
H OCH.sub.2 CH.sub.2 NMe.sub.2
H O H OMe OMe CH
I-968
H OCH.sub.2 CH.sub.2 OBu
H O H OMe Me CH
I-969
H OCH.sub.2 CH.sub.2 OBu
H O H OMe Me N
I-970
H OCH.sub.2 CH.sub.2 OBu
H O H OMe OMe CH
I-971
H OCH.sub.2 CH.sub.2 OBu
H O H OMe OMe N
I-972
H OCH.sub.2 CH.sub.2 OBu-t
H O H OMe Me CH
I-973
H OCH.sub.2 CH.sub.2 OBu-t
H O H OMe Me N
I-974
H OCH.sub.2 CH.sub.2 OBu-t
H O H OMe OMe CH
I-975
H OCH.sub.2 CH.sub.2 OBu-t
H O H OMe OMe N
I-976
H OCH.sub.2 CH.sub.2 OEt
H O H OMe Me CH
I-977
H OCH.sub.2 CH.sub.2 OEt
H O H OMe Me N
I-978
H OCH.sub.2 CH.sub.2 OEt
H O H OMe OMe CH
I-979
H OCH.sub.2 CH.sub.2 OMe
H O H OMe Me CH
I-980
H OCH.sub.2 CH.sub.2 OMe
H O H OMe OMe CH
I-981
H OCH.sub.2 CH.sub.2 OPh
H O H OMe OMe CH
I-982
H OCH.sub.2 CH.sub.2 OPr-i
H O H OMe Me CH
I-983
H OCH.sub.2 CH.sub.2 OPr-i
H O H OMe Me N
I-984
H OCH.sub.2 CH.sub.2 OPr-i
H O H OMe OMe CH
I-985
H OCH.sub.2 CH.sub.2 SMe
H O H Me OMe CH
I-986
H OCH.sub.2 CH.sub.2 SMe
H O H Me OMe N
I-987
H OCH.sub.2 CH.sub.2 SMe
H O H OMe OMe CH
I-988
H OCH.sub.2 CHCl.sub.2
H O H Me OMe CH
I-989
H OCH.sub.2 CHCl.sub.2
H O H Me OMe N
I-990
H OCH.sub.2 CHCl.sub.2
H O H OMe OMe CH
I-991
H OCH.sub.2 CHF.sub.2
H O H Me OMe CH
I-992
H OCH.sub.2 CHF.sub.2
H O H Me OMe N
I-993
H OCH.sub.2 CHF.sub.2
H O H OMe OMe CH
I-994
H OCH.sub.2 CN
H O H Me OMe CH
I-995
H OCH.sub.2 CN
H O H Me OMe N
I-996
H OCH.sub.2 CN
H O H OMe OMe CH
I-997
H OCH.sub.2 COOEt
H O H OMe OMe CH
I-998
H OCH.sub.2 COOMe
H O H Me OMe CH
I-999
H OCH.sub.2 COOMe
H O H Me OMe N
I-1000
H OCH.sub.2 COOMe
H O H OMe OMe CH
I-1001
H OCH.sub.2 COOPr
H O H Me OMe CH
I-1002
H OCH.sub.2 COOPr
H O H Me OMe N
I-1003
H OCH.sub.2 COOPr
H O H OMe OMe CH
I-1004
H OCH.sub.2 COOPr-i
H O H Me OMe CH
I-1005
H OCH.sub.2 COOPr-i
H O H Me OMe N
I-1006
H OCH.sub.2 COOPr-i
H O H OMe OMe CH
I-1007
H OCH.sub.2 OBn
H O H Me OMe CH
I-1008
H OCH.sub.2 OBn
H O H Me OMe N
I-1009
H OCH.sub.2 OBn
H O H OMe OMe CH
I-1010
H OCH.sub.2 OBu-t
H O H Me OMe CH
I-1001
H OCH.sub.2 OBu-t
H O H Me OMe N
I-1012
H OCH.sub.2 OBu-t
H O H OMe OMe CH
I-1013
H OCH.sub.2 OCH.sub.2 CF.sub.3
H O H Me OMe CH
I-1014
H OCH.sub.2 OCH.sub.2 CF.sub.3
H O H Me OMe N
I-1015
H OCH.sub.2 OCH.sub.2 CF.sub.3
H O H OMe OMe CH
I-1016
H OCH.sub.2 OCH.sub.2 CH.sub.2 OMe
H O H Me OMe CH
I-1017
H OCH.sub.2 OCH.sub.2 CH.sub.2 OMe
H O H Me OMe N
I-1018
H OCH.sub.2 OCH.sub.2 CH.sub.2 OMe
H O H OMe OMe CH
I-1019
H OCH.sub.2 OEt
H O H Me OMe CH
I-1020
H OCH.sub.2 OEt
H O H Me OMe N
I-1021
H OCH.sub.2 OEt
H O H OMe OMe CH
I-1022
H OCH.sub.2 OMe
H O H Me OMe CH
I-1023
H OCH.sub.2 OMe
H O H Me OMe N
I-1024
H OCH.sub.2 OMe
H O H OMe OMe CH
I-1025
H OCH.sub.2 SMe
H O H Me OMe CH
I-1026
H OCH.sub.2 SMe
H O H Me OMe N
I-1027
H OCH.sub.2 SMe
H O H OMe OMe CH
I-1028
H OCHF.sub.2 H O H Me OMe CH
I-1029
H OCHF.sub.2 H O H Me OMe N
I-1030
H OCHF2 H O H OMe OMe CH
I-1031
H OCOEt H O H Me OMe CH
I-1032
H OCOEt H O H Me OMe N
I-1033
H OCOEt H O H OMe OMe CH
I-1034
H OCOMe H O H OMe OMe CH
I-1035
H OCONMe.sub.2
H O H Me OMe CH
I-1036
H OCONMe.sub.2
H O H Me OMe N
I-1037
H OCONMe.sub.2
H O H OMe OMe CH
I-1038
H OCOPh H O H Me OMe CH
I-1039
H OCOPh H O H Me OMe N
I-1040
H OCOPh H O H OMe OMe CH
I-1041
H OCOPr H O H Me OMe CH
I-1042
H OCOPr H O H Me OMe N
I-1043
H OCOPr H O H OMe OMe CH
I-1044
H OEt H O H Me Me CH
I-1045
H OEt H O H OMe Me CH
I-1046
H OEt H O H OMe Me N
I-1047
H OEt H O H OMe OMe CH
I-1048
H OH H O H OMe OMe CH
I-1049
H OMe 5-Cl O H OMe Me N
I-1050
H OMe 5-Cl O H OMe OMe CH
I-1051
H OMe 5-OMe O H OMe Me CH
I-1052
H OMe H O H Cl OMe CH
I-1053
H OMe H O H OMe Me CH
I-1054
H OMe H O H OMe OMe N
I-1055
H OMe H O H Me Me CH
I-1056
H OMe H O H OMe Me N
I-1057
H OMe H O H OMe OMe CH
I-1058
H OPh H O H OMe OMe CH
I-1059
H OPh(2-Me) H O H OMe OMe CH
I-1060
H OPh(3-OMe) H O H OMe OMe CH
I-1061
H OPh(4-Cl) H O H OMe OMe CH
I-1062
H OPr H O H Cl OMe CH
I-1063
H OPr H O H Me Me CH
I-1064
H OPr H O H OMe Me CH
I-1065
H OPr H O H OMe Me N
I-1066
H OPr H O H OMe OMe CH
I-1067
H OPr-i H O H Me Me CH
I-1068
H OPr-i H O H OMe Me CH
I-1069
H OPr-i H O H OMe Me N
I-1070
H OPr-i H O H OMe OMe CH
I-1071
H Ph H O H OMe OMe CH
I-1072
H Pr H O H Me OMe CH
I-1073
H Pr H O H Me OMe N
I-1074
H Pr H O H OMe OMe CH
I-1075
H Pr-i H O H Me OMe CH
I-1076
H Pr-i H O H Me OMe N
I-1077
H Pr-i H O H OMe OMe CH
I-1078
H SBu H O H Cl OMe CH
I-1079
H SBu H O H OMe OMe CH
I-1080
H SCF.sub.3 H O H Me OMe CH
I-1081
H SCF.sub.3 H O H Me OMe N
I-1082
H SCF.sub.3 H O H OMe OMe CH
I-1083
H SCH.sub.2 CH.sub.2 Cl
H O H Me OMe CH
I-1084
H SCH.sub.2 CH.sub.2 Cl
H O H Me OMe N
I-1085
H SCH.sub.2 CH.sub.2 Cl
H O H OMe OMe CH
I-1086
H SCH.sub.2 CH.sub.2 F
H O H Me OMe CH
I-1087
H SCH.sub.2 CH.sub.2 F
H O H Me OMe N
I-1088
H SCH.sub.2 CH.sub.2 F
H O H OMe OMe CH
I-1089
H SEt H O H OMe Me N
I-1090
H SEt H O H OMe OMe CH
I-1091
H SH H O H OMe OMe CH
I-1092
H SMe H O H OMe OMe CH
I-1093
H SO.sub.2 Bu
H O H OMe OMe CH
I-1094
H SO.sub.2 CH.sub.2 CHCH.sub.2
H O H Me OMe CH
I-1095
H SO.sub.2 CH.sub.2 CHCH.sub.2
H O H Me OMe N
I-1096
H SO.sub.2 CH.sub.2 CHCH.sub.2
H O H OMe OMe CH
I-1097
H SO.sub.2 Et
H O H OMe OMe CH
I-1098
H SO.sub.2 Me
H O H OMe OMe CH
I-1099
H SO.sub.2 NMe.sub.2
H O H OMe OMe CH
I-1100
H SO.sub.2 NEt.sub.2
H O H Me OMe CH
I-1101
H SO.sub.2 NEt.sub.2
H O H Me OMe N
I-1102
H SO.sub.2 NEt.sub.2
H O H OMe OMe CH
I-1103
H SO.sub.2 NH.sub.2
H O H OMe OMe CH
I-1104
H SO.sub.2 NHBn
H O H OMe OMe CH
I-1105
H SO.sub.2 NHCH.sub.2 CCH
H O H OMe OMe CH
I-1106
H SO.sub.2 NHCH.sub.2 CHCH.sub.2
H O H OMe OMe CH
I-1007
H SO.sub.2 NHMe
H O H OMe OMe CH
I-1008
H SO.sub.2 NHOEt
H O H Me OMe CH
I-1009
H SO.sub.2 NHOEt
H O H Me OMe N
I-1110
H SO.sub.2 NHOEt
H O H OMe OMe CH
I-1111
H SO.sub.2 NHOMe
H O H OMe OMe CH
I-1112
H SO.sub.2 NHPh
H O H OMe OMe CH
I-1113
H SO.sub.2 Pr
H O H OMe OMe CH
I-1114
H SO.sub.2 Pr-i
H O H Cl OMe CH
I-1115
H SO.sub.2 Pr-i
H O H OMe OMe CH
I-1116
H SOEt H O H Me OMe CH
I-1117
H SOEt H O H Me OMe N
I-1118
H SOEt H O H OMe OMe CH
I-1119
H SOMe H O H OMe OMe CH
I-1120
H SPr H O H Cl OMe CH
I-1121
H SPr H O H OMe Me CH
I-1122
H SPr H O H OMe Me N
I-1123
H SPr H O H OMe OMe CH
I-1124
H SPr-i H O H Cl OMe CH
I-1125
H SPr-i H O H OMe OMe CH
I-1126
H NO.sub.2 H O H Me OMe N 182-184
I-1127
H SEt H O H Cl OMe CH
I-1128
H SEt H O H Me Me CH
I-1129
H SEt H O H OMe OMe N
I-1130
H SBu H O H OMe Me CH
I-1131
H Sbu H O H OMe Me N
I-1132
H SPr-i H O H OMe Me CH
I-1133
H SPr-i H O H OMe Me N
I-1134
H SOEt H O H OMe OMe N
I-1135
H SO.sub.2 Et
H O H OMe Me CH
I-1136
H SO.sub.2 Et
H O H OMe Me N
I-1137
H SO.sub.2 Et
H O H OMe Cl CH
I-1138
H SO.sub.2 Pr
H O H OMe Me CH
I-1139
H SO.sub.2 Pr
H O H OMe Me N
I-1140
H SO.sub.2 Pr
H O H OMe Cl CH
I-1141
H SO.sub.2 Bu
H O H OMe Me CH
I-1142
H SO.sub.2 Bu
H O H OMe Me N
I-1143
H SO.sub.2 Bu
H O H OMe Cl CH
I-1144
H SO.sub.2 Pr-i
H O H OMe Me CH
I-1145
H SO.sub.2 Pr-i
H O H OMe Me N
I-1146
H COOPr H O H OMe Me N
I-1147
H NO.sub.2 H O H OMe Cl CH
I-1148
H CONMe.sub.2
H O H OMe Me CH
I-1149
H Br H O H OMe Cl CH
I-1150
H
##STR29## H O H OMe OMe CH
I-1151
H OCH.sub.2 -Bu-t
H O H OMe OMe CH
I-1152
H OCH.sub.2 -Bu-t
H O H Me OMe CH
I-1153
H OCH.sub.2 CHCMe.sub.2
H O H OMe OMe CH
I-1154
H OCH.sub.2 CH.sub.2 CH.sub.2 F
H O H OMe OMe CH
I-1155
H OCH.sub.2 CH.sub.2 CH.sub.2 F
H O H Me OMe CH
I-1156
H OCH.sub.2 CH.sub.2 CH.sub.2 F
H O H Me OMe N
I-1157
H CH.sub.2 CH.sub.2 N.sub.3
H O H OMe OMe CH
I-1158
H
##STR30## H O H OMe OMe CH
I-1159
H COCF.sub.3 H O H OMe OMe CH
I-1160
H COOCH.sub.2 CHCHCl
H O H OMe OMe CH
I-1161
H SO.sub.2 CF.sub.3
H O H OMe OMe CH
I-1162
H OCOCF.sub.3
H O H OMe OMe CH
I-1163
H OCH.sub.2 OPh
H O H OMe OMe CH
I-1164
H CHNOH H O H OMe OMe CH
I-1165
H CHNOCH.sub.2 CHCH.sub.2
H O H OMe OMe CH
I-1166
H CHNOCH.sub.2 CCH
H O H OMe OMe CH
I-1167
H C(Me)NOBn H O H OMe OMe CH
I-1168
H C(Me)NOPh H O H OMe OMe CH
I-1169
H C(Bn)NOMe H O H OMe OMe CH
I-1170
H C(Ph)NOMe H O H OMe OMe CH
I-1171
H C(CF.sub.3)NOMe
H O H OMe OMe CH
I-1172
H COOCH.sub.2 CH.sub.2 Cl
H O H OMe OMe CH
I-1173
H COOCH.sub.2 CF.sub.3
H O H OMe OMe CH
I-1174
H Cl S-Cl O H OMe Me N
I-1175
H Cl 5-OMe O H OMe OMe CH
I-1176
H Cl 5-F O H OMe OMe CH
I-1177
H F 5-Cl O H OMe OMe CH
I-1178
H F 5-F O H OMe OMe CH
I-1179
H COOMe 5-Cl O H OMe OMe CH
I-1180
H COOEt 5-Cl O H OMe OMe CH
I-1181
H COOPr 5-Cl O H OMe OMe CH
I-1182
H COOPr-i 5-Cl O H OMe OMe CH
I-1183
H OMe 5-COOMe O H OMe OMe CH
I-1184
H COOMe 5-OMe O H OMe OMe CH
I-1185
H ONCHMe H O H OMe OMe CH
I-1186
H ONCMe.sub.2
H O H OMe OMe CH
I-1187
H ONCHBn H O H OMe OMe CH
I-1188
H OCH.sub.2 CH.sub.2 F
H O H OMe Me CH
I-1189
H OCH.sub.2 CH.sub.2 F
H O H OMe Me N
I-1190
H H 5-CN O H OMe OMe CH
I-1191
H H 5-CF.sub.3
O H OMe OMe CH
I-1192
H H 5-COOMe O H OMe OMe CH
I-1193
H H 5-COOEt O H OMe OMe CH
I-1194
H H 5-COOPr O H OMe OMe CH
I-1195
H H 5-COOPr-i
O H OMe OMe CH
I-1196
H H 5-COOCH.sub.2 CH.sub.2 Cl
O H OMe OMe CH
I-1197
H H 5-COOCH.sub.2 CH.sub.2 F
O H OMe OMe CH
I-1198
H H 5-COOCH.sub.2 CF.sub.3
O H OMe OMe CH
I-1199
H H 5-COOCH.sub.2 OMe
O H OMe OMe CH
I-1200
H H 5-CONMe.sub.2
O H OMe OMe CH
I-1201
H H 5-OCH.sub.2 CH.sub.2 F
O H OMe OMe CH
I-1202
H H 5-OCHF.sub.2
O H OMe OMe CH
I-1203
H H 5-OCH.sub.2 CF.sub.3
O H OMe OMe CH
I-1204
H H 5-OCH.sub.2 CH.sub.2 CH.sub.2 F
O H OMe OMe CH
I-1205
H H 5-OCH.sub.2 CHCH.sub.2
O H OMe OMe CH
I-1206
H H 5-OCH.sub.2 CCH
O H OMe OMe CH
I-1207
H H 5-NO.sub.2
O H OMe OMe CH
I-1208
H H 5-SMe O H OMe OMe CH
I-1209
H H 5-SEt O H OMe OMe CH
I-1210
H H 5-SPr O H OMe OMe CH
I-1211
H H 5-SPr-i O H OMe OMe CH
I-1212
H H 5-SO.sub.2 Et
O H OMe OMe CH
I-1213
H H 5-SO.sub.2 Pr
O H OMe OMe CH
I-1214
H H 5-SO.sub.2 Pr-i
O H OMe OMe CH
I-1215
H H 5-SOEt O H OMe OMe CH
I-1216
H H 5-Me O H OMe OMe CH
I-1217
H H 5-Et O H OMe OMe CH
I-1218
H H 5-Pr O H OMe OMe CH
I-1219
H H 5-SO.sub.2 NMe.sub.2
O H OMe OMe CH
I-1220
H H 5-OCF.sub.3
O H OMe OMe CH
I-1221
H H 5-CH.sub.2 CF.sub.3
O H OMe OMe CH
I-1222
H H 5-CH.sub.2 CHCH.sub.2
O H OMe OMe CH
I-1223
H H 5-COOMe O H OMe Me CH
I-1224
H H 5-COOMe O H OMe Me N
I-1225
H H 5-COOMe O H OMe OMe N
I-1226
H Cl H O CH.sub.3 OCH.sub.2
OMe OMe CH
I-1227
H Cl H O H OMe NMe.sub.2
N
I-1228
H Cl H O H OMe NHMe
N
I-1229
H
##STR31## H O H Me OMe CH
I-1230
H
##STR32## H O H Me OMe N
I-1231
H
##STR33## H O H OMe OMe CH
I-1232
H
##STR34## H O H OMe OMe CH
I-1233
H
##STR35## H O H Me OMe CH
I-1234
H
##STR36## H O H Me OMe N
I-1235
H
##STR37## H O H OMe OMe CH
I-1236
H
##STR38## H O H Me OMe CH
I-1237
H
##STR39## H O H Me OMe N
I-1238
H
##STR40## H O H OMe OMe CH
I-1239
H
##STR41## H O H Me OMe CH
I-1240
H
##STR42## H O H Me OMe N
I-1241
H OC.sub.2 H.sub.4O* O H OMe OMe CH
I-1242
H OC.sub.2 H.sub.4O* O H Me OMe CH
I-1243
H OC.sub.2 H.sub.4O* O H Me OMe N
I-1244
H SC.sub.2 H.sub.4S* O H OMe OMe CH
I-1245
H SC.sub.2 H.sub.4S* O H Me OMe CH
I-1246
H SC.sub.2 H.sub.4S* O H Me OMe N
I-1247
H OCH.sub.2O* O H OMe OMe CH
__________________________________________________________________________
*R.sup.3 represents the 5position.
TABLE 2
__________________________________________________________________________
##STR43##
Comp.
No. R.sup.1
R.sup.2 R.sup.3 X Y A B Z mp.(°C.)
__________________________________________________________________________
II-1
Me Ph H O H OMe OMe CH
II-2
Me Bn H O H OMe OMe CH
II-3
Me SH H O H OMe OMe CH
II-4
Me SMe H O H OMe OMe CH
II-5
Me SEt H O H OMe OMe CH
156-157
II-6
Me SPr H O H OMe OMe CH
143-145
II-7
Me SO.sub.2 Me
H O H OMe OMe CH
II-8
Me SO.sub.2 Et
H O H OMe OMe CH
196-198
II-9
Me SOMe H O H OMe OMe CH
II-10
Me SO.sub.2 NHMe
H O H OMe OMe CH
II-11
Me SO.sub.2 NHOMe
H O H OMe OMe CH
II-12
Me SO.sub.2 NMe.sub.2
H O H OMe OMe CH
169-171
II-13
Me SO.sub.2 NHBn
H O H OMe OMe CH
II-14
Me SO.sub.2 NHPh
H O H OMe OMe CH
II-15
Me SO.sub.2 NHCH.sub.2 CHCH.sub.2
H O H OMe OMe CH
II-16
Me SO.sub.2 NHCH.sub.2 C CH
H O H OMe OMe CH
II-17
H Cl H O H OMe OMe CH
191-193
II-18
Me Cl H O H Me Me CH
210-213
II-19
Me Cl 5-Cl O H OMe OMe CH
203-205
II-20
Et Cl H O H OMe OMe CH
174-175
II-21
Ph Cl H O H OMe OMe CH
221-223
II-22
Bn Cl H O H OMe OMe CH
II-23
Me H H O H OMe OMe CH
199-202
II-24
Me H H O H Me Me CH
208-210
II-25
Me H H O H OMe Me N 172-174
II-26
Me F H O H OMe OMe CH
205-206
II-27
Me Br H O H OMe OMe CH
179-182
II-28
Me Me H O H OMe OMe CH
178-180
II-29
Me CN H O H OMe OMe CH
189-191
II-30
Me CF.sub.3 H O H OMe OMe CH
II-31
Me Cl H O H OMe Me CH
202-204
II-32
Me Cl H O H OMe Me N 170-172
II-33
Me F H O H Me Me CH
207-209
II-34
Me F H O H OMe Me N 178-180
II-35
Me F H O H OMe Me CH
185-187
II-36
Me H 5-Cl O H OMe OMe CH
215-216
II-37
Me H 5-Cl O H Me Me CH
192-194
II-38
Me H 5-Cl O H OMe Me N 176-178
II-39
Me H 6-Cl O H OMe OMe CH
210-212
II-40
Me H 6-Cl O H Me Me CH
217-220
II-41
Me H 6-Cl O H OMe Me N 181-183
II-42
Me H 7-Cl O H OMe OMe CH
223-225
II-43
Me H 7-Cl O H OMe Me N 167-169
II-44
Me Cl H S H OMe OMe CH
II-45
Me Cl H O Me OMe OMe CH
II-46
Me COH H O H OMe OMe CH
II-47
Me COMe H O H OMe OMe CH
II-48
Me COEt H O H OMe OMe CH
II-49
Me COPh H O H OMe OMe CH
II-50
Me COCH.sub.2 CHCH.sub.2
H O H OMe OMe CH
II-51
Me COCH.sub.2 C CH
H O H OMe OMe CH
II-52
Me COBn H O H OMe OMe CH
II-53
Me NO.sub.2 H O H OMe OMe CH
155-157
II-54
Me NH.sub.2 H O H OMe OMe CH
II-55
Me NHMe H O H OMe OMe CH
143-144
II-56
Me NMe.sub.2 H O H OMe OMe CH
183-185
II-57
Me NHCOMe H O H OMe OMe CH
II-58
Me NHCOPh H O H OMe OMe CH
II-59
Me NHCOCH.sub.2 Cl
H O H OMe OMe CH
II-60
Me NHSO.sub.2 CH.sub.3
H O H OMe OMe CH
II-61
Me NHSO.sub.2 Ph
H O H OMe OMe CH
II-62
Me CO.sub.2 H H O H OMe OMe CH
II-63
Me CO.sub.2 Me
H O H OMe OMe CH
179-181
II-64
Me CO.sub.2 Et
H O H OMe OMe CH
181-182
II-65
Me CO.sub.2 Pr
H O H OMe OMe CH
188-190
II-66
Me CO.sub.2 Pr-i
H O H OMe OMe CH
200-202
II-67
Me CO.sub.2 Bu
H O H OMe OMe CH
189-190
II-68
Me CO.sub.2 Pen
H O H OMe OMe CH
II-69
Me CO.sub.2 Bn
H O H OMe OMe CH
II-70
Me CO.sub.2 Ph
H O H OMe OMe CH
II-71
Me CO.sub.2 CH.sub.2 CH.sub.2 F
H O H OMe OMe CH
II-72
Me CO.sub.2 CH.sub.2 CHCH.sub.2
H O H OMe OMe CH
II-73
Me CO.sub.2 CH.sub.2 C CH
H O H OMe OMe CH
II-74
Me CO.sub.2 Me
H O H OCHF.sub.2
OCHF.sub.2
CH
II-75
Me CO.sub.2 Et
H O H OCHF.sub.2
OCHF.sub.2
CH
II-76
Me CO.sub.2 Me
H O H OMe Cl CH
II-77
Me CO.sub.2 Me
H O H OMe Me CH
II-78
Me CO.sub.2 Me
H O H OMe Me N
II-79
Me CO.sub.2 Et
H O H OMe Me N
II-80
Me CO.sub.2 Me
H O H OMe OCHF.sub.2
CH
II-81
Me CO.sub.2 Me
5-F O H OMe OMe CH
II-82
Et CO.sub.2 Me
H O H OMe OMe CH
147-148
II-83
Bu CO.sub.2 Me
H O H OMe OMe CH
II-84
Bn CO.sub.2 Me
H O H OMe OMe CH
II-85
Ph CO.sub.2 Me
H O H OMe OMe CH
II-86
H CO.sub.2 Et
H O H OMe OMe CH
II-87
Me CO.sub.2 Me
H S H OMe OMe CH
II-88
Me CO.sub.2 Et
H S H OMe OMe CH
II-89
Me CO.sub.2 Me
H O Me OMe OMe CH
II-90
Me OH H O H OMe OMe CH
179-181
II-91
Me OMe H O H OMe OMe CH
162-165
II-92
Me OEt H O H OMe OMe CH
153-154
1I-93
Me OPr H O H OMe OMe CH
119-120
II-94
Me OPr-i H O H OMe OMe CH
176-179
II-95
Me OBu H O H OMe OMe CH
184-186
II-96
Me OBn H O H OMe OMe CH
200-203
II-97
Me OBn(4-Cl) H O H OMe OMe CH
II-98
Me OBn(3-OMe) H O H OMe OMe CH
II-99
Me OBn(2-Me) H O H OMe OMe CH
II-100
Me OPh H O H OMe OMe CH
II-101
Me OPh(4-Cl) H O H OMe OMe CH
II-102
Me OPh(3-OMe) H O H OMe OMe CH
II-103
Me OPh(2-Me) H O H OMe OMe CH
II-104
Me OCH.sub.2 CHCH.sub.2
H O H OMe OMe CH
133-136
II-105
Me OCH.sub.2 C CH
H O H OMe OMe CH
182-183
II-106
Me OCH.sub.2 CF.sub.3
H O H OMe OMe CH
165-170
II-107
Me OCH.sub.2 CH.sub.2 OMe
H O H OMe OMe CH
139-141
II-108
Me OCH.sub.2 CH.sub.2 OPh
H O H OMe OMe CH
II-109
Me OCOMe H O H OMe OMe CH
II-110
Me OMe H O H OMe Me CH
206-208
II-111
Me OMe H O H OMe Me N 198-201
II-112
Me OMe H O H Me Me CH
193-196
II-113
Me OEt H O H OMe Me N 179-181
II-114
Me OEt H O H OMe Me CH
174-175
II-115
Me OEt H O H Me Me CH
182-183
II-116
Me CONH.sub.2 H O H OMe OMe CH
II-117
Me CONHMe H O H OMe OMe CH
II-118
Me CONHEt H O H OMe OMe CH
II-119
Me CONHPr H O H OMe OMe CH
II-120
Me CONMe.sub.2
H O H OMe OMe CH
150-151
II-121
Me CONEt.sub.2
H O H OMe OMe CH
II-122
Me CONHBn H O H OMe OMe CH
II-123
Me CONHPh H O H OMe OMe CH
II-124
Me CONHCH.sub.2 CHCH.sub.2
H O H OMe OMe CH
II-125
Me CONHCH.sub.2 C CH
H O H OMe OMe CH
II-126
Me CONHOMe H O H OMe OMe CH
II-127
Me H 5-F O H OMe OMe CH
205-208
II-128
Me H 5-F O H Me Me CH
203-206
II-129
Me H 5-F O H OMe Me CH
186-189
II-130
Me H 5-F O H OMe Me N 175-179
II-131
H COOMe H O H OMe OMe CH
179-180
II-132
H COOMe H O H OMe Cl CH
193-194
II-133
H Cl H O H OMe Cl CH
178-181
II-134
Me Cl H O H OMe OMe CH
171-172
II-135
Me SO.sub.2 NH.sub.2
H O H OMe OMe CH
II-136
H Br H O H OMe OMe CH
190-193
II-137
Me H 5-OMe O H OMe OMe CH
178-181
II-138
Me H 5-OEt O H OMe OMe CH
188-189
II-139
Me H 5-OPr O H OMe OMe CH
197-198
II-140
Me OCH(CF.sub.3)Me
H O H OMe OMe CH
129-130
II-141
Me OCH.sub.2 CH.sub.2 Cl
H O H OMe OMe CH
182-186
II-142
Me OCH.sub.2 CH.sub.2 F
H O H OMe OMe CH
162-165
II-143
Me OCH.sub.2 CH.sub.2 OEt
H O H OMe OMe CH
138-139
II-144
Me OCH.sub.2 CH.sub.2 OPr-i
H O H OMe OMe CH
185-187
II-145
Me OCH.sub.2 CH.sub.2 OBu
H O H OMe OMe CH
120-121
II-146
Me OCH.sub.2 CH.sub.2 OBu-t
H O H OMe OMe CH
169-171
II-147
Me OCH.sub.2 COOEt
H O H OMe OMe CH
163-165
II-148
Me OCH.sub.2 CH.sub.2 NMe.sub.2
H O H OMe OMe CH
126-129
II-149
Me SBu H O H OMe OMe CH
156-158
II-150
Me SPr-i H O H OMe OMe CH
183-184
II-151
Me SO.sub.2 Pr
H O H OMe OMe CH
202-204
II-152
Me SO.sub.2 Bu
H O H OMe OMe CH
201-203
II-153
Me SO.sub.2 Pr-i
H O H OMe OMe CH
185-187
II-154
Me NHBn H O H OMe OMe CH
167-168
II-155
Me NEt.sub.2 H O H OMe OMe CH
173-175
II-156
Me OMe 5-Cl O H OMe OMe CH
211-212
II-157
Me Br H O H OMe Me CH
187-189
II-158
Et Cl H O H OMe Me CH
205-206
II-159
Ph Cl H O H OMe Me CH
215-217
II-160
Me OPr H O H OMe Me CH
174-175
II-161
Me OBu H O H OMe Me CH
169-171
II-162
Me OPr-i H O H OMe Me CH
157-159
II-163
Me H 5-OMe O H OMe Me CH
206-208
II-164
Me H 5-OEt O H OMe Me CH
174-176
II-165
Me H 5-OPr O H OMe Me CH
176-178
II-166
Me OCH.sub.2 CF.sub.3
H O H OMe Me CH
150-153
II-167
Me OCH(CF.sub.3)Me
H O H OMe Me CH
112-114
II-168
Me OCH.sub.2 CH.sub.2 OMe
H O H OMe Me CH
138-139
II-169
Me OCH.sub.2 CH.sub.2 OEt
H O H OMe Me CH
160-163
II-170
Me OCH.sub.2 CH.sub.2 OPr-i
H O H OMe Me CH
130-132
II-171
Me OCH.sub.2 CH.sub.2 OBu
H O H OMe Me CH
104-106
II-172
Me OCH.sub.2 CH.sub.2 OBu-t
H O H OMe Me CH
148-149
II-173
Me OCH.sub.2 CH.sub.2 NMe.sub.2
H O H OMe Me CH
126-129
II-174
Me SPr H O H OMe Me CH
164-165
II-175
Me CO.sub.2 Pr
H O H OMe Me CH
179-181
II-176
Me CO.sub.2 Pr-i
H O H OMe Me CH
187-190
II-177
Me CO.sub.2 Bu
H O H OMe Me CH
189-192
II-178
Me NO.sub.2 H O H OMe Me CH
161-163
II-179
Me CN H O H OMe Me CH
195-197
II-180
Me Br H O H OMe Me N 172-174
II-181
Et Cl H O H OMe Me N 192-194
II-182
Me OPr H O H OMe Me N 176-177
II-183
Me OBu H O H OMe Me N 143-145
II-184
Me OPr-i H O H OMe Me N 155-156
II-185
Me H 5-OMe O H OMe Me N 171-174
II-186
Me H 5-OEt O H OMe Me N 180-182
II-187
Me H 5-OPr O H OMe Me N 168-170
II-188
Me OCH.sub.2 CF.sub.3
H O H OMe Me N 168-170
II-189
Me OCH.sub.2 CH.sub.2 OEt
H O H OMe Me N 168-170
II-190
Me OCH.sub.2 CH.sub.2 OPr-i
H O H OMe Me N 153-155
II-191
Me OCH.sub.2 CH.sub.2 OBu
H O H OMe Me N 121-123
II-192
Me OCH.sub.2 CH.sub.2 OBu-t
H O H OMe Me N 161-162
II-193
Me OCH.sub.2 CH.sub.2 NMe.sub.2
H O H OMe Me N 119-121
II-194
Me SEt H O H OMe Me N 160-162
II-195
Me SPr H O H OMe Me N 129-131
II-196
Me NMe.sub.2 H O H OMe Me N 131-133
II-197
Me CO.sub.2 Pr-i
H O H OMe Me N 190-191
II-198
Me CO.sub.2 Bu
H O H OMe Me N 179-181
II-199
Me CN H O H OMe Me N 196-197
II-200
Me OMe 5-Cl O H OMe Me N 201-203
II-201
Me Cl H O H Cl OMe CH
187-189
II-202
Et Cl H O H Cl OMe CH
206-208
II-203
Ph Cl H O H Cl OMe CH
202-204
II-204
Me OMe H O H Cl OMe CH
220-223
II-205
Me OPr H O H Cl OMe CH
140-141
II-206
Me OBu H O H Cl OMe CH
153-154
II-207
Me H 5-OMe O H Cl OMe CH
174-177
II-208
Me OCH.sub.2 CF.sub.3
H O H Cl OMe CH
175-179
II-209
Me SPr H O H Cl OMe CH
165-167
II-210
Me SBu H O H Cl OMe CH
156-157
II-211
Me SPr-i H O H Cl OMe CH
177-179
II-212
Me SO.sub.2 Pr-i
H O H Cl OMe CH
184-186
II-213
Me NHBn H O H Cl OMe CH
160-163
II-214
Me NMe.sub.2 H O H Cl OMe CH
197-199
II-215
Et Cl H O H Me Me CH
229-231
II-216
Me OPr H O H Me Me CH
172-173
II-217
Me OBu H O H Me Me CH
148-149
II-218
Me OPr-i H O H Me Me CH
187-190
II-219
Me NMe.sub.2 H O H Me Me CH
174-176
II-220
Me OMe H O H OMe OMe N 193-195
II-221
Me H 5-OEt O H OMe OMe N 169-170
II-222
Me H 5-OPr O H OMe OMe N 168-169
II-223
Me OCH.sub.2 CH.sub.2 OBu
H O H OMe OMe N 132-133
II-224
Me OCH.sub.2 CH.sub.2 OBu-t
H O H OMe OMe N 162-163
II-225
Me NHMe H O H OMe Me CH
164-165
II-226
Me NHMe H O H OMe Me N 173-175
II-227
Me OMe 5-Cl O H OMe Me CH
222-225
II-228
Me OMe 5-OMe O H OMe OMe CH
168-170
II-229
Me OCHF.sub.2 H O H OMe OMe CH
179-181
II-230
Me OCHF.sub.2 H O H Me OMe CH
195-197
II-231
Me OCHF.sub.2 H O H Me OMe N 165-167
II-232
Me OCH.sub.2 CHF.sub.2
H O H OMe OMe CH
178-180
II-233
Me OCH.sub.2 CHF.sub.2
H O H Me OMe CH
180-182
II-234
Me OCH.sub.2 CHF.sub.2
H O H Me OMe N 164-166
II-235
Me OCH.sub.2 CH.sub.2 CF.sub.3
H O H OMe OMe CH
II-236
Me OCH.sub.2 CH.sub.2 CF.sub.3
H O H Me OMe CH
II-237
Me OCH.sub.2 CH.sub.2 CF.sub.3
H O H Me OMe N
II-238
Me OCH(CF.sub.2 CF.sub.3)Me
H O H OMe OMe CH
II-239
Me OCH(CF.sub.2 CF.sub.3)Me
H O H Me OMe CH
II-240
Me OCH(CF.sub.2 CF.sub.3)Me
H O H Me OMe N
II-241
Me OCH.sub.2 CF.sub.2 CHF.sub.2
H O H OMe OMe CH
II-242
Me OCH.sub.2 CF.sub.2 CHF.sub.2
H O H Me OMe CH
II-243
Me OCH.sub.2 CF.sub.2 CHF.sub.2
H O H Me OMe N
II-244
Me OCH.sub.2 CF.sub.2 CF.sub.3
H O H OMe OMe CH
II-245
Me OCH.sub.2 CF.sub.2 CF.sub.3
H O H Me OMe CH
II-246
Me OCH.sub.2 CF.sub.2 CF.sub.3
H O H Me OMe N
II-247
Me OCH.sub.2 CHCl.sub.2
H O H OMe OMe CH
II-248
Me OCH.sub.2 CHCl.sub.2
H O H Me OMe CH
II-249
Me OCH.sub.2 CHCl.sub.2
H O H Me OMe N
II-250
Me OCF.sub.2 CH.sub.2 Cl
H O H OMe OMe CH
II-251
Me OCF.sub.2 CH.sub.2 Cl
H O H Me OMe CH
II-252
Me OCF.sub.2 CH.sub.2 Cl
H O H Me OMe N
II-253
Me OCF.sub.2 CHFCl
H O H OMe OMe CH
II-254
Me OCF.sub.2 CHFCl
H O H Me OMe CH
II-255
Me OCF.sub.2 CHFCl
H O H Me OMe N
II-256
Me OCF.sub.3 H O H OMe OMe CH
II-257
Me OCF.sub.3 H O H Me OMe CH
II-258
Me OCF.sub.3 H O H Me OMe N
II-259
Me OCH.sub.2 CHCHCl
H O H OMe OMe CH
160-162
II-260
Me OCH.sub.2 CHCHCl
H O H Me OMe CH
II-261
Me OCH.sub.2 CHCHCl
H O H Me OMe N
II-262
Me OCH.sub.2 CHCCl.sub.2
H O H OMe OMe CH
II-263
Me OCH.sub.2 CHCCl.sub.2
H O H Me OMe CH
II-264
Me OCH.sub.2 CHCCl.sub.2
H O H Me OMe N
II-265
Me OCH.sub.2 C(Cl)CH.sub.2
H O H OMe OMe CH
160-162
II-266
Me OCH.sub.2 C(Cl)CH.sub.2
H O H Me OMe CH
II-267
Me OCH.sub.2 C(Cl)CH.sub.2
H O H Me OMe N
II-268
Me OCH.sub.2 C(Me)CH.sub.2
H O H OMe OMe CH
163-164
II-269
Me OCH.sub.2 C(Me)CH.sub.2
H O H Me OMe CH
II-270
Me OCH.sub.2 C(Me)CH.sub.2
H O H Me OMe N
II-271
Me OCH.sub.2 CHCHMe
H O H OMe OMe CH
II-272
Me OCH.sub.2 CHCHMe
H O H Me OMe CH
II-273
Me OCH.sub.2 CHCHMe
H O H Me OMe N
II-274
Me OCH.sub.2 CH.sub.2 N.sub.3
H O H OMe OMe CH
II-275
Me OCH.sub.2 CH.sub.2 N.sub.3
H O H Me OMe CH
II-276
Me OCH.sub.2 CH.sub.2 N.sub.3
H O H Me OMe N
II-277
Me OCH.sub.2 OMe
H O H OMe OMe CH
165-167
II-278
Me OCH.sub.2 OMe
H O H Me OMe CH
II-279
Me OCH.sub.2 OMe
H O H Me OMe N
II-280
Me OCH.sub.2 OEt
H O H OMe OMe CH
154-155
II-281
Me OCH.sub.2 OEt
H O H Me OMe CH
II-282
Me OCH.sub.2 OEt
H O H Me OMe N
II-283
Me OCH.sub.2 OBn
H O H OMe OMe CH
162-164
II-284
Me OCH.sub.2 OBn
H O H Me OMe CH
II-285
Me OCH.sub.2 OBn
H O H Me OMe N
II-286
Me OCH.sub.2 OCH.sub.2 CF.sub.3
H O H OMe OMe CH
II-287
Me OCH.sub.2 OCH.sub.2 CF.sub.3
H O H Me OMe CH
II-288
Me OCH.sub.2 OCH.sub.2 CF.sub.3
H O H Me OMe N
II-289
Me OCH.sub.2 OBu-t
H O H OMe OMe CH
II-290
Me OCH.sub.2 OBu-t
H O H Me OMe CH
II-291
Me OCH.sub.2 OBu-t
H O H Me OMe N
II-292
Me OCH.sub.2 OCH.sub.2 CH.sub.2 OMe
H O H OMe OMe CH
II-293
Me OCH.sub.2 OCH.sub.2 CH.sub.2 OMe
H O H Me OMe CH
II-294
Me OCH.sub.2 OCH.sub.2 CH.sub.2 OMe
H O H Me OMe N
II-295
Me OCH.sub.2 CN
H O H OMe OMe CH
II-296
Me OCH.sub.2 CN
H O H Me OMe CH
II-297
Me OCH.sub.2 CN
H O H Me OMe N
II-298
Me OCH.sub.2 COOMe
H O H OMe OMe CH
II-299
Me OCH.sub.2 COOMe
H O H Me OMe CH
II-300
Me OCH.sub.2 COOMe
H O H Me OMe N
II-301
Me OCH.sub.2 COOPr
H O H OMe OMe CH
II-302
Me OCH.sub.2 COOPr
H O H Me OMe CH
II-303
Me OCH.sub.2 COOPr
H O H Me OMe N
II-304
Me OCH.sub.2 COOPr-i
H O H OMe OMe CH
II-305
Me OCH.sub.2 COOPr-i
H O H Me OMe CH
II-306
Me OCH.sub.2 COOPr-i
H O H Me OMe N
II-307
Me OCH.sub.2 SMe
H O H OMe OMe CH
II-308
Me OCH.sub.2 SMe
H O H Me OMe CH
II-309
Me OCH.sub.2 SMe
H O H Me OMe N
II-310
Me OCH.sub.2 CH.sub.2 SMe
H O H OMe OMe CH
II-311
Me OCH.sub.2 CH.sub.2 SMe
H O H Me OMe CH
II-312
Me OCH.sub.2 CH.sub.2 SMe
H O H Me OMe N
II-313
Me SCF.sub.3 H O H OMe OMe CH
II-314
Me SCF.sub.3 H O H Me OMe CH
II-315
Me SCF.sub.3 H O H Me OMe N
II-316
Me SCH.sub.2 CH.sub.2 Cl
H O H OMe OMe CH
II-317
Me SCH.sub.2 CH.sub.2 Cl
H O H Me OMe CH
II-318
Me SCH.sub.2 CH.sub.2 Cl
H O H Me OMe N
II-319
Me SCH.sub.2 CH.sub.2 F
H O H OMe OMe CH
II-320
Me SCH.sub.2 CH.sub.2 F
H O H Me OMe CH
II-321
Me SCH.sub.2 CH.sub.2 F
H O H Me OMe N
II-322
Me SOEt H O H OMe OMe CH
II-323
Me SOEt H O H Me OMe CH
II-324
Me SOEt H O H Me OMe N
II-325
Me SO.sub.2 NHOEt
H O H OMe OMe CH
II-326
Me SO.sub.2 NHOEt
H O H Me OMe CH
II-327
Me SO.sub.2 NHOEt
H O H Me OMe N
II-328
Me SO.sub.2 CH.sub.2 CHCH.sub.2
H O H OMe OMe CH
II-329
Me SO.sub.2 CH.sub.2 CHCH.sub.2
H O H Me OMe CH
II-330
Me SO.sub.2 CH.sub.2 CHCH.sub.2
H O H Me OMe N
II-331
Me SO.sub.2 NEt.sub.2
H O H OMe OMe CH
II-332
Me SO.sub.2 NEt.sub.2
H O H Me OMe CH
II-333
Me SO.sub.2 NEt.sub.2
H O H Me OMe N
II-334
Me Et H O H OMe OMe CH
II-335
Me Et H O H Me OMe CH
II-336
Me Et H O H Me OMe N
II-337
Me Pr H O H OMe OMe CH
II-338
Me Pr H O H Me OMe CH
II-339
Me Pr H O H OMe OMe N
II-340
Me Pr-i H O H OMe OMe CH
II-341
Me Pr-i H O H Me OMe CH
II-342
Me Pr-i H O H Me OMe N
II-343
Me Bu H O H OMe OMe CH
II-344
Me Bu H O H Me OMe CH
II-345
Me Bu H O H Me OMe N
II-346
Me Bu-t H O H OMe OMe CH
II-347
Me Bu-t H O H Me OMe CH
II-348
Me Bu-t H O H Me OMe N
II-349
Me CH.sub.2 Cl
H O H OMe OMe CH
II-350
Me CH.sub.2 Cl
H O H Me OMe CH
II-351
Me CH.sub.2 Cl
H O H Me OMe N
II-352
Me CH.sub.2 F H O H OMe OMe CH
II-353
Me CH.sub.2 F H O H Me OMe CH
II-354
Me CH.sub.2 F H O H Me OMe N
II-355
Me CH.sub.2 OMe
H O H OMe OMe CH
II-356
Me CH.sub.2 OMe
H O H Me OMe CH
II-357
Me CH.sub.2 OMe
H O H Me OMe N
II-358
Me CH.sub.2 CF.sub.3
H O H OMe OMe CH
II-359
Me CH.sub.2 CF.sub.3
H O H Me OMe CH
II-360
Me CH.sub.2 CF.sub.3
H O H Me OMe N
II-361
Me
##STR44## H O H OMe OMe CH
II-362
Me
##STR45## H O H Me OMe CH
II-363
Me
##STR46## H O H Me OMe N
II-364
Me CH.sub.2 CH.sub.2 CF.sub.3
H O H OMe OMe CH
II-365
Me CH.sub.2 CH.sub.2 CF.sub.3
H O H Me OMe CH
II-366
Me CH.sub.2 CH.sub.2 CF.sub.3
H O H Me OMe N
II-367
Me CH.sub.2 CHCH.sub.2
H O H OMe OMe CH
II-368
Me CH.sub.2 CHCH.sub.2
H O H Me OMe CH
II-369
Me CH.sub.2 CHCH.sub.2
H O H Me OMe N
II-370
Me CH.sub.2 C CH
H O H OMe OMe CH
II-371
Me CH.sub.2 C CH
H O H Me OMe CH
II-372
Me CH.sub.2 C CH
H O H Me OMe N
II-373
Me CH.sub.2 COOMe
H O H OMe OMe CH
II-374
Me CH.sub.2 COOMe
H O H Me OMe CH
II-375
Me CH.sub.2 COOMe
H O H Me OMe N
II-376
Me CH.sub.2 COOEt
H O H OMe OMe CH
II-377
Me CH.sub.2 COOEt
H O H Me OMe CH
II-378
Me CH.sub.2 COOEt
H O H Me OMe N
II-379
Me CH.sub.2 CN
H O H OMe OMe CH
II-380
Me CH.sub.2 CN
H O H Me OMe CH
II-381
Me CH.sub.2 CN
H O H Me OMe N
II-382
Me CH.sub.2 CONMe.sub.2
H O H OMe OMe CH
II-383
Me CH.sub.2 CONMe.sub.2
H O H Me OMe CH
II-384
Me CH.sub.2 CONMe.sub.2
H O H Me OMe N
II-385
Me CH.sub.2 SO.sub.2 NMe.sub.2
H O H OMe OMe CH
II-386
Me CH.sub.2 SO.sub.2 NMe.sub.2
H O H Me OMe CH
II-387
Me CH.sub.2 SO.sub.2 NMe.sub.2
H O H Me OMe N
II-388
Me CH.sub.2 NMe.sub.2
H O H OMe OMe CH
II-389
Me CH.sub.2 NMe.sub.2
H O H Me OMe CH
II-390
Me CH.sub.2 NMe.sub.2
H O H Me OMe N
II-391
Me CHCH.sub.2 H O H OMe OMe CH
II-392
Me CHCH.sub.2 H O H Me OMe CH
II-393
Me CHCH.sub.2 H O H Me OMe N
II-394
Me CHCHMe H O H OMe OMe CH
II-395
Me CHCHMe H O H Me OMe CH
II-396
Me CHCHMe H O H Me OMe N
II-397
Me C CH H O H OMe OMe CH
II-398
Me C CH H O H Me OMe CH
II-399
Me C CH H O H Me OMe N
II-400
Me C CMe H O H OMe OMe CH
II-401
Me C CMe H O H Me OMe CH
II-402
Me C CMe H O H Me OMe N
II-403
Me CHCHCOOMe H O H OMe OMe CH
II-404
Me CHCHCOOMe H O H Me OMe CH
II-405
Me CHCHCOOMe H O H Me OMe N
II-406
Me CH(Me)COMe H O H OMe OMe CH
II-407
Me CH(Me)COMe H O H Me OMe CH
II-408
Me CH(Me)COMe H O H Me OMe N
II-409
Me CH(Me)COEt H O H OMe OMe CH
II-410
Me CH(Me)COEt H O H Me OMe CH
II-411
Me CH(Me)COEt H O H Me OMe N
II-412
Me CH(Et)COMe H O H OMe OMe CH
II-413
Me CH(Et)COMe H O H Me OMe CH
II-414
Me CH(Et)COMe H O H Me OMe N
II-415
Me CH(Et)COEt H O H OMe OMe CH
II-416
Me CH(Et)COEt H O H Me OMe CH
II-417
Me CH(Et)COEt H O H Me OMe N
II-418
Me
##STR47## H O H OMe OMe CH
II-419
Me
##STR48## H O H Me OMe CH
II-420
Me
##STR49## H O H Me OMe N
II-421
Me COPr H O H OMe OMe CH
II-422
Me COPr H O H Me OMe CH
II-423
Me COPr H O H Me OMe N
II-424
Me COPr-i H O H OMe OMe CH
II-425
Me COPr-i H O H Me OMe CH
II-426
Me COPr-i H O H Me OMe N
II-427
Me CHNOMe H O H OMe OMe CH
II-428
Me CHNOMe H O H Me OMe CH
II-429
Me CHNOMe H O H Me OMe N
II-430
Me CHNOEt H O H OMe OMe CH
II-431
Me CHNOEt 11 O H Me OMe CH
II-432
Me CHNOEt H O H Me OMe N
II-433
Me C(Me)NOMe H O H OMe OMe CH
II-434
Me C(Me)NOMe H O H Me OMe CH
II-435
Me C(Me)NOMe H O H Me OMe N
II-436
Me C(Me)NOEt H O H OMe OMe CH
II-437
Me C(Me)NOEt H O H Me OMe CH
II-438
Me C(Me)NOEt H O H Me OMe N
II-439
Me C(Me)NOPr H O H OMe OMe CH
II-440
Me C(Me)NOPr H O H Me OMe CH
II-441
Me C(Me)NOPr H O H Me OMe N
II-442
Me C(Me)NOCH.sub.2 CH.sub.2 Cl
H O H OMe OMe CH
II-443
Me C(Me)NOCH.sub.2 CH.sub.2 Cl
H O H Me OMe CH
II-444
Me C(Me)NOCH.sub.2 CH.sub.2 Cl
H O H Me OMe N
II-445
Me C(Me)NOCH.sub.2 CH.sub.2 F
H O H OMe OMe CH
II-446
Me C(Me)NOCH.sub.2 CH.sub.2 F
H O H Me OMe CH
II-447
Me C(Me)NOCH.sub.2 CH.sub.2 F
H O H Me OMe N
II-448
Me NHEt H O H OMe OMe CH
II-449
Me NHEt H O H Me OMe CH
II-450
Me NHEt H O H Me OMe N
II-451
Me NHPr H O H OMe OMe CH
II-452
Me NHPr H O H Me OMe CH
II-453
Me NHPr H O H Me OMe N
II-454
Me NHCOOMe H O H OMe OMe CH
II-455
Me NHCOOMe H O H Me OMe CH
II-456
Me NHCOOMe H O H Me OMe N
II-457
Me NHCOOEt H O H OMe OMe CH
II-458
Me NHCOOEt H O H Me OMe CH
II-459
Me NHCOOEt H O H Me OMe N
II-460
Me NHCOOPh H O H OMe OMe CH
II-461
Me NHCOOPh H O H Me OMe CH
II-462
Me NHCOOPh H O H Me OMe N
II-463
Me N(Me)SO.sub.2 Me
H O H OMe OMe CH
II-464
Me N(Me)SO.sub.2 Me
H O H Me OMe CH
II-465
Me N(Me)SO.sub.2 Me
H O H Me OMe N
II-466
Me N(Et)SO.sub.2 Me
H O H OMe OMe CH
II-467
Me N(Et)SO.sub.2 Me
H O H Me OMe CH
II-468
Me N(Et)SO.sub.2 Me
H O H Me OMe N
II-469
Me N(Me)SO.sub.2 Et
H O H OMe OMe CH
II-470
Me N(Me)SO.sub.2 Et
H O H Me OMe CH
II-471
Me N(Me)SO.sub.2 Et
H O H Me OMe N
II-472
Me N(Et)SO.sub.2 Et
H O H OMe OMe CH
II-473
Me N(Et)SO.sub.2 Et
H O H Me OMe CH
II-474
Me N(Et)SO.sub.2 Et
H O H Me OMe N
II-475
Me NHCOEt H O H OMe OMe CH
II-476
Me NHCOEt H O H Me OMe CH
II-477
Me NHCOEt H O H Me OMe N
II-478
Me NHCOCF.sub.3
H O H OMe OMe CH
II-479
Me NHCOCF.sub.3
H O H Me OMe CH
II-480
Me NHCOCF.sub.3
H O H Me OMe N
II-481
Me NCHMe H O H OMe OMe CH
II-482
Me NCHMe H O H Me OMe CH
II-483
Me NCHMe H O H Me OMe N
II-484
Me NCHPh H O H OMe OMe CH
II-485
Me NCHPh H O H Me OMe CH
II-486
Me NCHPh H O H Me OMe N
II-487
Me N.sub.3 H O H OMe OMe CH
II-488
Me N.sub.3 H O H Me OMe CH
II-489
Me N.sub.3 H O H Me OMe N
II-490
Me I H O H OMe OMe CH
II-491
Me I H O H Me OMe CH
II-492
Me I H O H Me OMe N
II-493
Me OCOEt H O H OMe OMe CH
II-494
Me OCOEt H O H Me OMe CH
II-495
Me OCOEt H O H Me OMe N
II-496
Me OCOPr H O H OMe OMe CH
II-497
Me OCOPr H O H Me OMe CH
II-498
Me OCOPt H O H Me OMe N
II-499
Me OCOPh H O H OMe OMe CH
II-500
Me OCOPh H O H Me OMe CH
II-501
Me OCOPh H O H Me OMe N
II-502
Me OCONMe.sub.2
H O H OMe OMe CH
II-503
Me OCONMe.sub.2
H O H Me OMe CH
II-504
Me OCONMe.sub.2
H O H Me OMe N
II-505
Me Cl H O H CF.sub.3
OMe CH
II-506
Me OPr-i H O H Cl OMe CH
II-507
Me SEt H O H Me OMe CH
II-508
Me SEt H O H Cl OMe CH
II-509
Me SEt H O H Me Me CH
II-510
Me SEt H O H OMe OMe N
II-511
Me SBu H O H OMe Me CH
II-512
Me SBu H O H OMe Me N
II-513
Me SPr-i H O H OMe Me CH
II-514
Me SPr-i H O H OMe Me N
II-515
Me SOEt H O H OMe OMe N
II-516
Me SO.sub.2 Et
H O H OMe Me CH
II-517
Me SO.sub.2 Et
H O H OMe Me N
II-518
Me SO.sub.2 Et
H O H OMe Cl CH
II-519
Me SO.sub.2 Pr
H O H OMe Me CH
II-520
Me SO.sub.2 Pr
H O H OMe Me N
II-521
Me SO.sub.2 Pr
H O H OMe Cl CH
II-522
Me SO.sub.2 Bu
H O H OMe Me CH
II-523
Me SO.sub.2 Bu
H O H OMe Me N
II-524
Me SO.sub.2 Bu
H O H OMe Cl CH
II-525
Me SO.sub.2 Pr-i
H O H OMe Me CH
II-526
Me SO.sub.2 Pr-i
H O H OMe Me N
II-527
Me COOPr H O H OMe Me N
II-528
Me NO.sub.2 H O H OMe Cl CH
II-529
Me CONMe.sub.2
H O H OMe Me CH
II-530
Me Br H O H OMe Cl CH
II-531
Me
##STR50## H O H OMe OMe CH
156-158
II-532
Me OCH.sub.2 Bu-t
H O H OMe OMe CH
144-146
II-533
Me OCH.sub.2 Bu-t
H O H Me OMe CH
126-128
II-534
Me OCH.sub.2 CHCMe.sub.2
H O H OMe OMe CH
164-166
II-535
Me OCH.sub.2 CH.sub.2 CH.sub.2 F
H O H OMe OMe CH
136-138
II-536
Me OCH.sub.2 CH.sub.2 CH.sub.2 F
H O H Me OMe CH
173-175
II-537
Me OCH.sub.2 CH.sub.2 CH.sub.2 F
H O H Me OMe N 160-163
II-538
Me CH.sub.2 CH.sub.2 N.sub.3
H O H OMe OMe CH
II-539
Me
##STR51## H O H OMe OMe CH
II-540
Me COCF.sub.3 H O H OMe OMe CH
II-541
Me COOCH.sub.2 CHCHCl
H O H OMe OMe CH
II-542
Me SO.sub.2 CF.sub.3
H O H OMe OMe CH
II-543
Me OCOCF.sub.3
H O H OMe OMe CH
II-544
Me OCH.sub.2 OPh
H O H OMe OMe CH
II-545
Me CHNOH H O H OMe OMe CH
II-546
Me CHNOCH.sub.2 CHCH.sub.2
H O H OMe OMe CH
II-547
Me CHNOCH.sub.2 C CH
H O H OMe OMe CH
II-548
Me C(Me)NOBn H O H OMe OMe CH
II-549
Me C(Me)NOPh H O H OMe OMe CH
II-550
Me C(Bn)NOMe H O H OMe OMe CH
II-551
Me C(Ph)NOMe H O H OMe OMe CH
II-552
Me C(CF.sub.3)NOMe
H O H OMe OMe CH
II-553
Me COOCH.sub.2 CH.sub.2 Cl
H O H OMe OMe CH
II-554
Me COOCH.sub.2 CF.sub.3
H O H OMe OMe CH
II-555
Me Cl 5-Cl O H OMe Me N
II-556
Me Cl 5-OMe O H OMe OMe CH
197-199
II-557
Me Cl 5-F O H OMe OMe CH
II-558
Me F 5-Cl O H OMe OMe CH
II-559
Me F 5-F O H OMe OMe CH
II-560
Me COOMe 5-Cl O H OMe OMe CH
II-561
Me COOEt 5-Cl O H OMe OMe CH
II-562
Me COOPr 5-Cl O H OMe OMe CH
II-563
Me COOPr-i 5-Cl O H OMe OMe CH
II-564
Me OMe 5-COOMe O H OMe OMe CH
II-565
Me COOMe 5-OMe O H OMe OMe CH
II-566
Me H 5-CN O H OMe OMe CH
II-567
Me H 5-CF.sub.3
O H OMe OMe CH
II-568
Me H 5-COOMe O H OMe OMe CH
II-569
Me H 5-COOEt O H OMe OMe CH
II-570
Me H 5-COOPr O H OMe OMe CH
II-571
Me H 5-COOPr-i
O H OMe OMe CH
II-572
Me H 5-COOCH.sub.2 CH.sub.2 Cl
O H OMe OMe CH
II-573
Me H 5-COOCH.sub.2 CH.sub.2 F
O H OMe OMe CH
II-574
Me H 5-COOCH.sub.2 CF.sub.3
O H OMe OMe CH
II-575
Me H 5-COOCH.sub.2 OMe
O H OMe OMe CH
II-576
Me H 5-CONMe.sub.2
O H OMe OMe CH
II-577
Me H 5-OCH.sub.2 CH.sub.2 F
O H OMe OMe CH
II-578
Me H 5-OCHF.sub.2
O H OMe OMe CH
II-579
Me H 5-OCH.sub.2 CF.sub.3
O H OMe OMe CH
II-580
Me H 5-OCH.sub.2 CH.sub.2 CH.sub.2 F
O H OMe OMe CH
II-581
Me H 5-OCH.sub.2 CHCH.sub.2
O H OMe OMe CH
II-582
Me H 5-OCH.sub.2 C CH
O H OMe OMe CH
II-583
Me H 5-NO.sub.2
O H OMe OMe CH
II-584
Me H 5-SMe O H OMe OMe CH
II-585
Me H 5-SEt O H OMe OMe CH
II-586
Me H 5-SPr O H OMe OMe CH
II-587
Me H 5-SPr-i O H OMe OMe CH
II-588
Me H 5-SO.sub.2 Et
O H OMe OMe CH
II-589
Me H 5-SO.sub.2 Pr
O H OMe OMe CH
II-590
Me H 5-SO.sub.2 Pr-i
O H OMe OMe CH
II-591
Me H 5-SOEt O H OMe OMe CH
II-592
Me H 5-Me O H OMe OMe CH
II-593
Me H S-Et O H OMe OMe CH
II-594
Me H 5-Pr O H OMe OMe CH
II-595
Me H 5-SO.sub.2 NMe.sub.2
O H OMe OMe CH
II-596
Me H 5-OCF.sub.3
O H OMe OMe CH
II-597
Me H 5-CH.sub.2 CF.sub.3
O H OMe OMe CH
II-598
Me H 5-CH.sub.2 CHCH.sub.2
O H OMe OMe CH
II-599
Me H 5-COOMe O H OMe Me CH
II-600
Me H 5-COOMe O H OMe Me N
II-601
Me H 5-COOMe O H OMe OMe N
II-602
Me
##STR52## H O H OMe OMe CH
II-603
Me
##STR53## H O H Me OMe CH
II-604
Me
##STR54## H O H Me OMe N
II-605
Me
##STR55## H O H OMe OMe CH
II-606
Me
##STR56## H O H Me OMe CH
II-607
Me
##STR57## H O H Me OMe N
II-608
Me
##STR58## H O H OMe OMe CH
II-609
Me
##STR59## H O H Me OMe CH
II-610
Me
##STR60## H O H Me OMe N
II-611
Me OC.sub.2 H.sub.4 O*
O H OMe OMe CH
II-612
Me OC.sub.2 H.sub.4 O*
O H Me OMe CH
II-613
Me OC.sub.2 H.sub.4 O*
O H Me OMe N
II-614
Me SC.sub.2 H.sub.4 S*
O H OMe OMe CH
II-615
Me SC.sub.2 H.sub.4 S*
O H Me OMe CH
II-616
Me SC.sub.2 H.sub.4 S*
O H Me OMe N
II-617
Me OCH.sub.2 O*
O H OMe OMe CH
II-618
##STR61##
Cl H O H OMe OMe CH
II-619
##STR62##
Cl H O H OMe OMe CH
II-620
##STR63##
Cl H O H OMe OMe CH
II-621
COMe Cl H O H OMe OMe CH
II-622
COEt Cl H O H OMe OMe CH
II-623
COPr Cl H O H OMe OMe CH
II-624
COPr-i Cl H O H OMe OMe CH
II-625
COPh Cl H O H OMe OMe CH
II-626
SO.sub.2 Me
Cl H O H OMe OMe CH
II-627
SO.sub.2 Et
Cl H O H OMe OMe CH
II-628
SO.sub.2 Ph
Cl H O H OMe OMe CH
II-629
COOMe Cl H O H OMe OMe CH
II-630
COOEt Cl H O H OMe OMe CH
II-631
COOPh Cl H O H OMe OMe CH
II-632
CONMe.sub.2
Cl H O H OMe OMe CH
II-633
SO.sub.2 NMe.sub.2
Cl H O H OMe OMe CH
II-634
Ph Cl H O H Me OMe N
II-635
CH.sub.2 OMe
Cl H O H OMe OMe CH
II-636
CH.sub.2 OBn
Cl H O H OMe OMe CH
II-637
CH.sub.2 CH.sub.2 F
Cl H O H OMe OMe CH
II-638
CH.sub.2 CH.sub.2 Cl
Cl H O H OMe OMe CH
II-639
CF.sub.3
Cl H O H OMe OMe CH
II-640
CH.sub.2 F
Cl H O H OMe OMe CH
II-641
CH.sub.2 CHCH.sub.2
OMe H O H OMe OMe CH
II-642
COCF.sub.3
Cl H O H OMe OMe CH
II-643
##STR64##
Cl H O H OMe OMe CH
II-644
Me Cl H O CH.sub.3 OCH.sub.2
OMe OMe CH
II-645
Me Cl H O H OMe NMe.sub.2
N
II-646
Me Cl H O H OMe NHMe N
II-648
Me ONCHMe H O H OMe OMe CH
II-649
Me ONCMe.sub.2
H O H OMe OMe CH
II-650
Me ONCHBn H O H OMe OMe CH
II-651
Me OCH.sub.2 CH.sub.2 F
H O H OMe Me CH
167-170
II-652
Me OCH.sub.2 CH.sub.2 F
H O H OMe Me N 167-169
II-653
Me F H O H NMe.sub.2
OCH.sub.2 CF.sub.3
N 108-112
II-654
Me SO.sub.2 NMe.sub.2
H O H OMe Me N 191-193
II-655
Me CO.sub.2 CH.sub.2 CH.sub.2 Cl
H O H OMe OMe CH
II-656
Me CO.sub.2 CH.sub.2 CF.sub.3
H O H OMe OMe CH
II-657
Me CO.sub.2 CH.sub.2 OMe
H O H OMe OMe CH
II-658
H CO.sub.2 CH.sub.2 CH.sub.2 Cl
H O H OMe OMe CH
II-659
H CO.sub.2 CH.sub.2 CF.sub.3
H O H OMe OMe CH
II-660
H CO.sub.2 CH.sub.2 OMe
H O H OMe OMe CH
__________________________________________________________________________
*R.sup.3 represents the 5 position.
The following processes may, for example, be mentioned as the processes for producing the compounds of the present invention. However, the processes are not limited to such specific processes.
Common processes for producing the compound I! or II! of the present invention are shown by the following Processes 1 to 3. ##STR65## (wherein R1, R2, R3, A, B, Z, X and Y have the same meanings as defined above.)
Namely, the compound of the present invention represented by the formula I! or II! can be produced by reacting an intermediate for its production of the present invention represented by the formula I-a! or II-a! (hereinafter referred to as an intermediate, and the process for its production will be described hereinafter) and a compound represented by the formula III!.
This reaction is usually conducted in a solvent or without solvent, if necessary, in the presence of a base. The range of the reaction temperature is a range from -20° C. to the boiling point of the solvent, and the range of the reaction time is a range of from 0.5 hour to 24 hours. With respect to the amounts of the compounds to be subjected to the reaction, the amounts of the compound represented by the formula III! and the base are respectively independently from 1 to 1.5 equivalent relative to one equivalent of the intermediate represented by the formula I-a! or II-a!.
As the solvent, an aromatic hydrocarbon such as benzene, xylene or toluene, a halogenated hydrocarbon such as chloroform, carbon tetrachloride, dichloroethane, chlorobenzene or dichlorobenzene, an ether such as diethyl ether, dioxane, tetrahydrofuran (THF), isopropyl ether (IPE) or diethylene glycol dimethyl ether, an alcohol such as methanol, ethanol or 2-propanol, an ester such as ethyl acetate or butyl acetate, a nitro compound such as nitromethane or nitrobenzene, a nitrile such as acetonitrile or isobutyronitrile, or an aprotic polar solvent such as formamide, N,N-dimethylformamide (DMF), N,N-dimethylacetamide (DMAC), dimethylsulfoxide (DMSO) or N-methylpyrrolidone (NMP), may, for example, be mentioned.
As the base, an organic base such as pyridine, triethylamine, 1,4-diazabicyclo 2.2.2!octane, 1,8-diazabicyclo 5.4.0!-7-undecene (DBU), N,N-diethylaniline or diethyl-methylamine, an inorganic base such as sodium hydroxide, potassium hydroxide, sodium carbonate, potassium carbonate or sodium hydride, or an alkali metal alkoxide such as sodium methoxide or sodium ethoxide, may, for example, be mentioned.
Further, the compound represented by the formula III! can be produced by reacting a compound represented by the formula IV! in Process 2 with phenyl chloroformate, phenyl chlorothio-O-formate or phenyl chlorodithioformate, in a proper solvent in the presence of a base. ##STR66## (wherein R1, R2, R3, A, B, X, Y and Z have the same meanings as defined above.)
The compound of the present invention represented by the formula I! or II! can be produced by reacting a compound represented by the formula I-b! or II-b! and a compound represented by the formula IV!. The compound represented by the formula I-b! or II-b! can be produced by reacting an intermediate represented by the formula I-a! or II-a! with phosgene or thiophosgene in a suitable solvent.
This reaction is usually conducted in a solvent or without solvent, if necessary, in the presence of a base. The range of the reaction temperature, the range of the reaction time, and the solvent and the base to be used in the reaction are the same as in Process 1. With respect to the amounts of the compounds to be subjected to the reaction, the amounts of the compounds represented by the formula IV! and the base are respectively independently from 1 to 1.5 equivalent relative to one equivalent of the compound represented by the formula I-b! or II-b!. ##STR67## (wherein R1, R2, R3, A, B, X, Y and Z have the same meanings as defined above.)
The compound of the present invention represented by the formula I! or II! can be produced by reacting a compound represented by the formula I-c! or II-c! and a compound of the formula IV!. The compound represented by the formula I-c! or II-c! can be produced by reacting an intermediate represented by the formula I-a! or II-a! with phenyl chloroformate, phenyl chlorothio-O-formate or phenyl chlorodithioformate, in a suitable solvent in the presence of a base. It may also be produced by reacting a compound represented by the formula I-b! or II-b! with phenol or thiophenol.
This reaction is usually conducted in a solvent or without solvent, if necessary, in the presence of a base. The range of the reaction temperature, the range of the reaction time, and the solvent and the base to be used in the reaction are the same as in Process 1. With respect to the amounts of the compounds to be subjected to the reaction, the amounts of the compound represented by the formula IV! and the base are respectively independently from 1 to 1.5 equivalent relative to one equivalent of the compound represented by the formula I-c! or II-c!. A process for producing an intermediate of the formula I-a! useful for the production of the compound of the present invention will be shown by Process 1 For Producing An Intermediate, and a process for producing an intermediate of the formula II-a! will be shown by Process 2 For Producing An Intermediate. However, the processes are not limited to such specific examples. ##STR68## (wherein R1 represents a hydrogen atom, an alkyl group, a benzyl group or a phenyl group, R2 and R3 represent a hydrogen atom, an alkyl group, a halogen atom, a nitro group, an alkoxy group, a haloalkoxy group or a haloalkyl group, and L represents a halogen atom.)
Namely, a compound represented by the formula V! is reacted with the corresponding hydrazine derivative, for example, in DMSO, to obtain a compound represented by the formula VI!. Further, in concentrated hydrochloric acid, a diazonium salt is formed, and this is reacted with sulfurous acid gas in a solvent such as acetic acid in the presence of copper chloride to obtain a compound represented by the formula VII!. This is reacted with excess t-butylamine to produce a compound represented by the formula I-d!. Then, the t-butyl group is removed with excess trifluoroacetic acid to obtain an intermediate represented by the formula I-a!. ##STR69## (wherein R1 represents an alkyl group, a haloalkyl group, a benzyl group or a phenyl group, and R2 and R3 represent a hydrogen atom, an alkyl group, a halogen atom, an alkoxy group, a phenyl group, a benzyl group or a haloalkoxy group.)
Namely, a compound represented by the formula IX! can be produced by reacting a compound represented by the formula VIII! with n-butyl lithium, for example, in ethyl ether, within a temperature range of from -40° to -20° C., followed by blowing in sulfurous acid gas. An intermediate represented by the formula II-a! can be produced by adding an aqueous solution of the compound represented by the formula IX! to an aqueous solution of a mixture of hydroxylamine-o-sulfonic acid and a base under cooling with ice.
In this reaction formula, the compound of the formula VIII! can be produced by a method disclosed in a known literature such as Liebigs Ann. Chem., 908 (1980)!, Org. Synth. Coll. Vol. V, 650!, J. Chem. Soc. Perkin Trans. II, 1695, (1975)!, or Org. Synth, Coll. Vol. V, 941!.
The intermediate represented by the formula I-a! or II-a! can be produced also by the following process. ##STR70## (wherein R1 represents an alkyl group, a cycloalkyl group, a haloalkyl group, an alkoxyalkyl group, a benzyloxyalkyl group, a benzyl group, a dialkylaminocarbonyl group, an alkoxycarbonyl group, a alkylsulfonyl group, a phenylsulfonyl group, a dialkylaminosulfonyl group, a haloalkylcarbonyl group, an alkylcarbonyl group, a benzoyl group or an alkenyl group, R2 or R3 represents a hydrogen atom, a halogen atom, an alkoxy group, a haloalkoxy group, a haloalkyl group, an alkoxycarbonyl group, a phenyl group or a benzyl group, L represents a halogen atom, and M represents a bromine atom or a chlorine atom.)
Namely, a compound represented by the formula X! is reacted with N-bromosuccinimide, N-chlorosuccinimide, or bromine or chlorine in carbon tetrachloride in the presence of a light and a radical reaction initiating agent to obtain a compound represented by the formula XI!. The compound represented by the formula XI! is reacted with thiourea to obtain a compound represented by the formula XII!. The compound represented by the formula XII! is reacted with chlorine or bromine in a mixed solution of acetic acid and water to obtain a compound represented by the formula XIII!. Then, this compound is reacted with t-butylamine to obtain a compound represented by the formula XIV!. The compound represented by the formula XIV! is reduced to obtain a compound represented by the formula XV!. The compound represented by the formula XV! and isoamylnitrous acid are reacted, followed by reaction with hydrochloric acid to obtain a compound represented by the formula XVI!. The compound represented by the formula XVI! is reacted with e.g. an alkyl halide or a benzyl halide to obtain a compound represented by the formula I-d! or II-d!.
The compound represented by the formula XVI!, I-d! or II-d! can be converted to a compound represented by the formula XVII! and an intermediate represented by the formula I-a! or II-a!, respectively, by removing the t-butyl group with trifluoroacetic acid, as shown in Process 1 For Producing An Intermediate.
Further, the compound represented by the formula XVII! is reacted with R1 L (wherein R1 and L have the same meanings as defined above) to obtain intermediates of the formulas I-a! and II-a!.
The intermediate represented by the formula I-a! may be prepared by various processes depending upon the types of the substituents. However, it can be produced by the processes represented by the following Process 4 For Producing An Intermediate and Processes 5-1 to 5-3 For Producing An Intermediate. ##STR71## (wherein R1 represents a hydrogen atom, an alkyl group, a benzyl group or a phenyl group, R2 represents a halogen atom, preferably a fluorine atom, R3 has the same meaning as defined above, and R4 represents an alkoxy group, an alkoxyalkoxy group, a benzyloxy group, a cycloalkylalkoxy group, a haloalkoxy group, a dialkylaminoalkoxy group, an alkylthio group, an alkylamino group, a dialkylamino group or a benzylamino group.)
Namely, in this reaction, an intermediate represented by the formula I-a! or II-a! is reacted with a compound represented by the formula R4 -H (wherein R4 has the same meaning as defined above) in a polar solvent such as DMSO, DMF, DMAC or NMP in the presence of a base such as sodium hydride, potassium hydride, potassium carbonate, potassium t-butoxide, sodium hydroxide or potassium hydroxide, to obtain an intermediate represented by the formula I-e! or II-e!, respectively. ##STR72## (wherein R1 represents an alkyl group, a benzyl group or a phenyl group, R3 has the same meaning as defined above, R5 represents an alkyl group, a benzyl group, an alkenyl group, an alkynyl group, a haloalkenyl group, a haloalkyl group, an alkoxyalkyl group, an alkoxycarbonylalkyl group or a cyanoalkyl group, and L1 represents a halogen atom, an alkylsulfonyloxy group, a haloalkylsulfonyloxy group or a benzenesulfonyloxy group which may be substituted.)
Namely, in this reaction formula, an intermediate represented by the formula I-f! or II-f! is reacted with a compound represented by the formula R5 -L1 (wherein R5 and L1 have the same meanings as defined above) in a suitable solvent in the presence of a base, to obtain an intermediate represented by the formula I-g! or II-g!, respectively.
The intermediate represented by the formula I-f! or II-f! can be produced by the following process. ##STR73## (wherein R1 represents an alkyl group, a benzyl group or a phenyl group, R2 represents a halogen atom, preferably a fluorine atom, R3 represents a hydrogen atom, a halogen atom, an alkyl group, a haloalkyl group, a haloalkoxy group or an alkoxy group, and R8 represents an alkyl group, a benzyl group or a cycloalkyl group, preferably a cyclopropylmethyl group.)
Namely, in this reaction formula, an intermediate represented by the formula I-a! or II-a! is reacted with a compound of the formula R8 --OH (wherein R8 has the same meaning as defined above) in a suitable solvent in the presence of a base, to obtain an intermediate represented by the formula I-h! or II-h!, which is further subjected to removal of the protecting group to obtain an intermediate of the formula I-f! or II-f!, respectively. ##STR74## (wherein R1 represents an alkyl group, a benzyl group or a phenyl group, and R3 and R5 have the same meanings as defined above.)
Namely, in this reaction formula, an intermediate represented by the formula I-f! or II-f! is subjected to a Mitsunobu reaction (as disclosed in Organic Reactions Vol. 42, p-335) using a compound represented by the formula R5 --OH (wherein R5 has the same meaning as defined above) in a suitable solvent, to obtain an intermediate of the formula I-g! or II-g!, respectively. ##STR75## (wherein R1 represents an alkyl group, a benzyl group or a phenyl group, R3, R5 and L1 have the same meanings as defined above, and R6 represents an alkyl group, preferably a methyl group.)
Namely, in this reaction formula, an intermediate represented by the formula I-f! or II-f! is reacted with acetal of DMF to obtain a compound represented by the formula I-i! or II-i!, which is then reacted with a compound represented by the formula R5 -L1 (wherein R5 and L1 have the same meanings as defined above) in a suitable solvent in the presence of a base to obtain a compound represented by the formula I-j! or II-j!, which is then hydrolyzed with an acid or alkali to obtain an intermediate represented by the formula I-g! or II-g!.
Now, specific compounds of the intermediate represented by the formula I-a! or II-a! will be listed in Table 3.
TABLE 3
______________________________________
Inter-
mediate
No. R.sup.1
R.sup.2 R.sup.3 mp. (°C.)
______________________________________
##STR76##
1 Me Ph H
2 Me Bn H
3 Me SH H
4 Me SMe H
5 Me SEt H 223-225
6 Me SPr H 208-209
7 Me SO.sub.2 Me H
8 Me SO.sub.2 Et H 271-273
9 Me SOMe H
10 Me SO.sub.2 NHMe H
11 Me SO.sub.2 NHOMe H
12 Me SO.sub.2 NMe.sub.2
H 248-252
13 Me SO.sub.2 NHBn H
14 Me SO.sub.2 NHPh H
15 Me SO.sub.2 NHCH.sub.2 CHCH.sub.2
H
16 Me SO.sub.2 NHCH.sub.2 C CH
H
17 H Cl H 215-217
18 Me Cl H 268-270
19 Me Cl 5-Cl 283-285
20 Et Cl H 180-182
21 Ph Cl H
22 Bn Cl H
23 Me H H 178-180
24 Me F H 221-223
25 Me Br H 285-287
26 Me Me H
27 Me CN H 274-281
28 Me CF.sub.3 H
29 Me H 5-Cl
30 Me H 6-Cl
31 Me H 7-Cl
32 Me COH H
33 Me COMe H
34 Me COEt H
35 Me COPh H
36 Me CO.sub.2 CH.sub.2 CHCH.sub.2
H
37 Me CO.sub.2 CH.sub.2 C CH
H
38 Me COBn H
39 Me NO.sub.2 H 249-251
40 Me NH.sub.2 H
41 Me NHMe H
42 Me NMe.sub.2 H
43 Me NHCOMe H
44 Me NHCOPh H
45 Me NHCOCH.sub.2 Cl H
46 Me NHSO.sub.2 CH.sub.3
H
47 Me NHSO.sub.2 Ph H
48 Me CO.sub.2 H H
49 Me CO.sub.2 Me H 233-234
50 Me CO.sub.2 Et H 193-195
51 Me CO.sub.2 Pr H 185-188
52 Me CO.sub.2 Pr-i H 219-220
53 Me CO.sub.2 Bu H 167-168
54 Me CO.sub.2 Pen H
55 Me CO.sub.2 Bn H
56 Me CO.sub.2 Ph H
57 Me CO.sub.2 CH.sub.2 CH.sub.2 F
H
58 Me CO.sub.2 Me 5-F
59 Et CO.sub.2 Me H
60 Bu CO.sub.2 Me H
61 Bn CO.sub.2 Me H
62 Ph CO.sub.2 Me H
63 H CO.sub.2 Et H
64 Me OH H
65 Me OMe H 268-270
66 Me OEt H 230-233
67 Me OPr H 210-212
68 Me OPr-i H 200-201
69 Me OBu H 203-205
70 Me OBn H
71 Me OBn(4-Cl) H
72 Me OBn(3-OMe) H
73 Me OBn(2-Me) H
74 Me OPh H
75 Me OPh(4-Cl) H
76 Me OPh(3-OMe) H
77 Me OPh(2-Me) H
78 Me OCH.sub.2 CHCH.sub.2
H
79 Me OCH.sub.2 C CH H
80 Me OCH.sub.2 CF.sub.3
H
81 Me OCH.sub.2 CH.sub.2 OMe
H
82 Me OCH.sub.2 CH.sub.2 OPh
H
83 Me OCOMe H
84 Me CONH.sub.2 H
85 Me CONHMe H
86 Me CONHEt H
87 Me CONHPr H
88 Me CONMe.sub.2 H 274-275
89 Me CONEt.sub.2 H
90 Me CONHBn H
91 Me CONHPh H
92 Me CONHCH.sub.2 CHCH.sub.2
H
93 Me CONHCH.sub.2 C CH
H
94 Me CONHOMe H
95 Me H 5-F
96 Me SO.sub.2 NH.sub.2
H
97 Me SPr-i H 228-231
98 Me OCH.sub.2 CH.sub.2 OEt
H
99 Me OCH.sub.2 CH.sub.2 OPr-i
H
100 Me OCH.sub.2 CH.sub.2 OBu
H
101 Me OCH.sub.2 CH.sub.2 OBu-t
H
102 Me OCH.sub.2 CH.sub.2 NMe.sub.2
H
103 Me OCH.sub.2 COOEt H
104 Me OCH.sub.2 CH.sub.2 Cl
H
105 Me OCH.sub.2 CH.sub.2 F
H
106 Me OCH.sub.2 OCH.sub.3
H
167 Me OCH(CF.sub.3)Me H
108 Me H 5-OMe
109 Me H 5-OEt
110 Me H 5-OPr
111 Et CO.sub.2 Me H
112 Et Br H
113 Me OCHF.sub.2 H
114 Me SO.sub.2 Pr H 270-272
115 Me SO.sub.2 Pr-i H 260-263
116 Me SO.sub.2 Bu H 287-290
117 Me SBu H 187-189
118 Me OMe 5-Cl
119 Me NHBn H
120 Me OCH.sub.2 Bu-t H
121 Me OCH.sub.2 CHF.sub.2
H
122 H NO.sub.2 H >300
123 H Br H 183-186
124 H COOCH.sub.3 H 243-247
125 Me H 5-CO.sub.2 Me
238-241
##STR77##
126 Me Ph H
127 Me Bn H
128 Me SH H
129 Me SMe H
130 Me SEt H 145-147
131 Me SPr H
132 Me SO.sub.2 Me H
133 Me SO.sub.2 Et H 167-169
134 Me SOMe H
135 Me SO.sub.2 NHMe H
136 Me SO.sub.2 NHOMe H
137 Me SO.sub.2 NMe.sub.2
H 218-220
138 Me SO.sub.2 NHBn H
139 Me SO.sub.2 NHPh H
140 Me SO.sub.2 NHCH.sub.2 CHCH.sub.2
H
141 Me SO.sub.2 NHCH.sub.2 C CH
H
142 H Cl H 215-217
143 Me Cl H 173-175
144 Me Cl 5-Cl
145 Et Cl H 182-184
146 Ph Cl H 220-221
147 Bn Cl H
148 Me H H 181-183
149 Me F H 151-152
150 Me Br H 182-183
151 Me Me H 149-151
152 Me CN H 227-228
153 Me CF.sub.3 H
154 Me H 5-Cl 186-188
155 Me H 6-Cl 206-207
156 Me H 7-Cl 175-177
157 Me COH H
158 Me COMe H
159 Me COEt H
160 Me COPh H
161 Me CO.sub.2 CH.sub.2 CHCH.sub.2
H
162 Me CO.sub.2 CH.sub.2 C CH
H
163 Me COBn H
164 Me NO.sub.2 H 193-194
165 Me NH.sub.2 H
166 Me NHMe H 179-181
167 Me NMe.sub.2 H 197-200
168 Me NHCOMe H
169 Me NHCOPh H
170 Me NHCOCH.sub.2 Cl H
171 Me NHSO.sub.2 CH.sub.3
H
172 Me NHSO.sub.2 Ph H
173 Me CO.sub.2 H H
174 Me CO.sub.2 Me H 160-163
175 Me CO.sub.2 Et H 135-137
176 Me CO.sub.2 Pr H 130-132
177 Me CO.sub.2 Pr-i H 145-147
178 Me CO.sub.2 Bu H 113-114
179 Me CO.sub.2 Pen H
180 Me CO.sub.2 Bn H
181 Me CO.sub.2 Ph H
182 Me CO.sub.2 CH.sub.2 CH.sub.2 F
H
183 Me CO.sub.2 Me 5-F
184 Et CO.sub.2 Me H
185 Bu CO.sub.2 Me H
186 Bn CO.sub.2 Me H
187 Ph CO.sub.2 Me H
188 H CO.sub.2 Et H
189 Me OH H 180-181
190 Me OMe H 265-268
191 Me OEt H 184-185
192 Me OPr H 186-188
193 Me OPr-i H 205-206
194 Me OBu H 152-154
195 Me OBn H
196 Me OBn(4-Cl) H
197 Me OBn(3-OMe) H
198 Me OBn(2-Me) H
199 Me OPh H
200 Me OPh(4-Cl) H
201 Me OPh(3-OMe) H
202 Me OPh(2-Me) H
203 Me OCH.sub.2 CHCH.sub.2
H 143-144
204 Me OCH.sub.2 C CH H 180-181
205 Me OCH.sub.2 CF.sub.3
H 182-183
206 Me OCH.sub.2 CH.sub.2 OMe
H 174-176
207 Me OCH.sub.2 CH.sub.2 OPh
H
208 Me OCOMe H
209 Me CONH.sub.2 H
210 Me CONHMe H
211 Me CONHEt H
212 Me CONHPr H
213 Me CONMe.sub.2 H 267-270
214 Me CONHEt.sub.2 H
215 Me CONHBn H
216 Me CONHPh H
217 Me CONHCH.sub.2 CHCH.sub.2
H
218 Me CONHCH.sub.2 C CH
H
219 Me CONHOMe H
220 Me H 5-F 174-175
221 Me SO.sub.2 NH.sub.2
H
222 Me SPr-i H 134-135
223 Me OCH.sub.2 CH.sub.2 OEt
H 116-120
224 Me OCH.sub.2 CH.sub.2 OPr-i
H 118-119
225 Me OCH.sub.2 CH.sub.2 OBu
H 144-145
226 Me OCH.sub.2 CH.sub.2 OBu-t
H 183-184
227 Me OCH.sub.2 CH.sub.2 NMe.sub.2
H 184-187
228 Me OCH.sub.2 COOEt H 116-120
229 Me OCH.sub.2 CH.sub.2 Cl
H 177-179
230 Me OCH.sub.2 CH.sub.2 F
H 178-180
231 Me OCH.sub.2 OCH.sub.3
H 163-165
232 Me OCH(CF.sub.3)Me H 165-167
233 Me H 5-OMe 169-172
234 Me H 5-OEt 152-153
235 Me H 5-OPr 149-151
236 Et CO.sub.2 Me H 123-125
237 Et Br H
238 Me OCHF.sub.2 H 164-166
239 Me SO.sub.2 Pr H 176-178
240 Me SO.sub.2 Pr-i H 220-221
241 Me SO.sub.2 Bu H 156-158
242 Me SBu H 162-164
243 Me OMe 5-Cl 161-163
244 Me NHBn H 189-191
245 Me OCH.sub.2 Bu-t H 207-208
246 Me OCH.sub.2 CHF.sub.2
H 186-188
247 Me OCH.sub.2 CH.sub.2 CH.sub.2 F
H 139-140
248 Me OMe H 138-140
249 Me Cl H 176-178
250 Me OCH.sub.2 OEt H 148-150
251 Me OCH.sub.2 C(CH.sub.3)CH.sub.2
H 132-134
252 Me OCH.sub.2 CHC(Me).sub.2
H 141-143
253 Me OCH.sub.2 CHCHCl
H 164-166
254 Me
##STR78## H 139-141
255 Me OCH.sub.2 OBn H 156-158
______________________________________
Now, the present invention will be specifically explained by describing the process for producing the intermediate and the process for producing the compound of the present invention as Preparation Examples.
75 g (539 mmol) of 2,6-difluorobenzonitrile was added to 300 ml of DMSO, and 33 g (716 mmol) of methylhydrazine was dropwise added thereto with stirring. The reaction proceeded exothermically, and the dropwise addition was continued while maintaining the temperature at a level of from 80° to 100° C. After returning to room temperature, the mixture was poured into a large excess amount of cool water, whereupon crystals were collected by filtration and dried in air to obtain 72 g (yield: 81%) of 3-amino-1-methyl-4-fluoro-1H-indazole (compound represented by the formula VI! (slightly yellow crystals).
Then, 70 g (424 mmol) of 3-amino-1-methyl-4-fluoro-1H-indazole was dissolved in 200 ml of acetic acid, and 140 ml of concentrated hydrochloric acid was added thereto. The mixture was vigorously stirred, and a solution having 33 g (478 mmol) of sodium nitrite dissolved in 60 ml of water, was gradually dropwise added thereto within a range of from -5° to -10° C. The diazonium salt solution thus obtained, was gradually dropwise added to a mixture having 17 g (100 mmol) of cupric chloride dihydrate added to a solution obtained by blowing sulfurous acid gas into 370 ml of acetic acid until saturation (120 g). After completion of the dropwise addition, stirring was continued for one hour at a temperature of not higher than 0° C., and then the mixture was poured into a large excess amount of cold water, whereupon crystals were collected by filtration and dried in air to obtain 70 g (yield: 66%) of 1-methyl-4-fluoro-1H-indazole-3-sulfonylchloride (compound represented by the formula VII!) (slightly purple crystals).
Further, 13.9 g (56 mmol) of 1-methyl-4-fluoro-1H-indazole-3-sulfonylchloride in 50 ml of THF, was added to 12.9 g (177 mmol) of t-butylamine in 100 ml of THF, and the mixture was stirred at room temperature overnight. After completion of the reaction, the mixture was poured into a large excess amount of water, whereupon the crystals were collected by filtration and dried in air to obtain 15.9 g (yield: 99.6%) of 3-(N-t-butylsulfamoyl)-1-methyl-4-fluoro-1H-indazole (compound represented by the formula I-d!) (slightly purple crystals).
15 g (53 mmol) of 3-(N-t-butylsulfamoyl)-1-methyl-4-fluoro-1H-indazole was added to 50 ml of trifluoroacetic acid, and the mixture was stirred overnight. After completion of the reaction, trifluoroacetic acid was distilled off under reduced pressure, and the residue was washed with n-hexane to obtain 10.5 g (yield: 86.8%) of 1-methyl-4-fluoro-1H-indazole-3-sulfonamide (slightly purple crystals). Melting point: 221°-223° C.
0.35 g (2.3 mmol) of DBU was added to a solution containing 0.5 g (2.3 mmol) of 1-methyl-4-fluoro-1H-indazole-3-sulfonamide obtained in Preparation Example 1 and 0.62 g (2.3 mmol) of phenyl (4,6-dimethoxypyrimidin-2-yl)carbamate in 20 ml of acetonitrile, and the mixture was stirred at room temperature for 12 hours. The mixture was poured into ice water and acidified with citric acid, whereupon the formed crystals were collected by filtration and washed with ice water, IPE and ethyl ether to obtain 0.49 g (yield: 52%) of the desired product (colorless needle like crystals). Melting point: 205°-209° C.
A suspension containing 98 g (0.5 mol) of methyl 2-methyl-3-nitrobenzoate, 100 g (0.56 mol) of N-bromosuccinimide and 1 g of benzoyl peroxide in carbon tetrachloride (800 ml), was refluxed for 3 days under irradiation with 500 W. The suspension was cooled to room temperature and subjected to filtration, whereupon the filtrate was concentrated. To the residue, ethyl ether (200 ml) and IPE (200 ml) were added, whereupon the formed crystals were collected by filtration to obtain 121 g (yield: 88.3%) of the desired product. Melting point: 65°-67° C.
In methanol (2 l), 207 g (0.76 mol) of the product from Preparation Example 3-1 and 57.6 g (0.76 mol) of thiourea were refluxed for 12 hours. After cooling, methanol was distilled off, and ethyl acetate (1 l) was added to the residue. The product was subjected to filtration. This product was used for the subsequent reaction without purification. The obtained amount: 246 g (yield: 93%)
110 g (0.32 mol) of the product from Preparation Example 3-2 in water (2 l) and acetic acid (1 l), was cooled to 5° C. and chlorine was blown thereto for 4 hours at a temperature of from 5° to 10° C. And, the mixture was stirred at room temperature for one hour. Then, the product was collected by filtration and washed with ice water and then dissolved in 1 l of dichloromethane. To this solution, 54 g (0.74 mol) of t-butylamine was dropwise added at a temperature of from 0° to 5° C. Then, the mixture was stirred at room temperature for 2 hours. The organic layer was washed with water and then concentrated. IPE was added to the residue, followed by filtration to obtain 63 g (yield: 60.1%) of the desired product. This product was used for the subsequent reaction without purification.
A solution containing 48 g (0.145 mol) of the product from Preparation Example 3-3 and 164 g (0.73 mol) of stannous chloride dihydrate in 300 ml of ethanol, was refluxed for 2 hours. After cooling, it was added to 2 l of ethyl acetate, and powdery sodium hydrogencarbonate (500 g) was gradually added thereto. The formed salt was collected by filtration and thoroughly washed with ethyl acetate. The organic layer was concentrated to obtain 35.9 g (yield: 82.4%) of the desired product. Melting point: 123°-125° C.
A suspension containing 30 g (0.1 mol) from Preparation Example 3-4, 30.6 g (0.3 mol) of acetic anhydride and 10 g (0.102 mol) of potassium acetate in benzene (500 ml), was heated to 80° C., and at the same temperature, 17.6 g (0.15 mol) of isoamyl nitrite was dropwise added thereto. Further, the mixture was refluxed for 12 hours and then cooled, and the salt was filtered. The organic layer was concentrated, and methanol (500 ml) and 10% hydrochloric acid (20 ml) were added to the residue, and the mixture was refluxed for one hour. After distilling off methanol, water was added thereto, and the mixture was neutralized with an aqueous sodium hydrogencarbonate solution. The formed crystals were collected by filtration to obtain 29.3 g (yield: 94.1%) of the desired product. Melting point: 218°-220° C.
6.8 g (48 mmol) of methyl iodide was added to a solution containing 10 g (32 mmol) of the product from Preparation Example 3-5 and 6.6 g (48 mmol) of potassium carbonate in methanol (200 ml), and the mixture was refluxed for 3 hours. Methanol was distilled off, and water was added to the residue, and the mixture was extracted with ethyl acetate. The organic layer was washed with water, dried over anhydrous magnesium sulfate, then concentrated and purified by silica gel column chromatography to obtain 5.9 g (yield; 56.8%; melting point: 189°-190° C.) of methyl 3-(t-butylaminosulfonyl)-1-methyl-1H-indazole-4-carboxylate and 2.1 g (yield: 19.8%; melting point: 147°-148° C.) of methyl 3-(t-butylaminosulfonyl) 2-methyl-2H-indazole-4-carboxylate.
A solution containing 9.5 g (72 mmol) of 2-methyl-2H-indazole in 200 ml of ethyl ether, was cooled to -30° C., and 61.4 g (144 mmol) of n-butyl lithium (a 15% hexane solution) was dropwise added thereto. The mixture was stirred for one hour at the same temperature, and then an excess amount of sulfurous acid gas was blown thereinto for 3 hours at a temperature of not higher than -20° C. After completion of the reaction, the mixture was returned to room temperature, stirred for 12 hours and then diluted with ethyl ether. The product was subjected to filtration. The crystals were dried to obtain crude lithium 2-methyl-2H-indazole-3-sulfinate. This product was used for the subsequent reaction without purification. 48.8 g (430 mmol) of hydroxylamine-O-sulfonic acid was gradually added to a solution containing 17.2 g (430 mmol) of sodium hydroxide in water (300 ml) under cooling with ice (not higher than 10° C.). This solution was added all at once to a solution containing the crude lithium 2-methyl-2H-indazole-3-sulfinate previously prepared in water (100 ml), and then the mixture was stirred for 12 hours at room temperature. Formed crystals were collected by filtration to obtain 8.8 g (yield: 58%) of 2-methyl-2H-indazole-3-sulfonamide (slightly yellow granular crystals). Melting point: 181°-183° C.
2.3 g (15 mmol) of DBU was added to a solution containing 3.2 g (15 mmol) of 2-methyl-2H-indazole-3-sulfonamide obtained in Preparation Example 4 and 4.1 g (15 mmol) of phenyl (4,6-dimethoxypyrimidin-2-yl)carbamate in acetonitrile (50 ml), and the mixture was stirred at room temperature for 12 hours. The mixture was poured into ice water and acidified with citric acid. Formed crystals were collected by filtration and washed with ice water, IPE and ethyl ether, to obtain 4.0 g (yield: 68%) of the desired product (colorless needle like crystals). Melting point: 199°-202° C.
A solution containing 5 g (21.8 mmol) of 4-fluoro-1-methyl-1H-indazole-3-sulfonamide and 12.6 g of sodium methoxide (a 28% methanol solution) (65 mmol) in DMSO (50 ml), was stirred at 130° C. for one hour. After confirming the disappearance of the starting material by thin layer chromatography (TLC), the mixture was poured into ice water and acidified with citric acid. Formed crystals were collected by filtration and washed with water and IPE to obtain 3.2 g (yield: 60.9%) of the desired product. Melting point: 268°-270° C.
4.8 g (77 mmol) of ethanethiol was added to a solution containing 8.6 g (77 mmol) of potassium t-butoxide in DMSO (70 ml), under cooling with ice, and 8 g (35 mmol) of 4-fluoro-2-methyl-2H-indazole-3-sulfonamide was further added thereto. This mixture was stirred at 120° C. for 2 hours. After confirming the disappearance of the starting material by TLC, treatment was conducted in the same manner as in Preparation Example 6 to obtain 6.8 g (yield: 72.5%) of the desired product. Melting: 145°-147° C.
2.8 g (70 mmol) of 60% sodium hydride was suspended in 50 ml of DMSO, and 6 g (83 mmol) of cyclopropane methanol was dropwise added thereto. The mixture was stirred at room temperature for one hour, and then 5.4 g (24 mmol) of 4 -fluoro-2 -methyl-2H-indazole-3-sulfonamide was added thereto. The mixture was stirred at 130° C. for 3 hours. After the reaction, the mixture was poured into ice water, acidified with citric acid and extracted with ethyl acetate. The organic layer was washed with water and then concentrated. Formed crystals were collected by filtration, washed with IPE and then dried to obtain 5.8 g (yield: 90%) of the desired product. Melting point: 139°-141° C.
A mixture comprising 62 g (221 mmol) of 4-cyclopropylmethoxy-2-methyl-2H-indazole-3-sulfonamide, 120 ml of acetic acid and 120 ml of concentrated hydrochloric acid, was stirred at 80° C. for one hour. After concentrating acetic acid-hydrochloric acid, the mixture was poured into ice water. Crystals were collected by filtration and washed with water. Further, the crystals were washed with IPE and dried to obtain 35.1 g (yield: 70%) of the desired product. Melting point: 180°-181° C.
1.3 g of allyl bromide was added to a mixture comprising 5 g (22 mmol) of 4-hydroxy-2-methyl-2H-indazole-3-sulfonamide and 50 ml of a DMF solution of 1.9 g (22 mmol) of sodium hydrogencarbonate, and the mixture was stirred at room temperature for 12 hours. The mixture was poured into ice water, acidified with citric acid and extracted with ethyl acetate. The organic layer was washed, then concentrated and purified by column chromatography (hexane/ethyl acetate=2/1) to obtain 1.9 g (yield: 32.5%) of the desired product. Melting point: 143°-144° C.
3.8 g (22 mmol) of diethylazo dicarboxylate was added to a solution containing 5 g (22 mmol) of 4-hydroxy-2-methyl-2H-indazole-3-sulfonamide, 1.8 g (22 mmol) of 2-chloroethanol and 5.8 g (22 mmol) of triphenylphosphine in 50 ml of THF, and the mixture was stirred at room temperature for 20 hours. The mixture was poured into water and extracted with ethyl acetate. The organic layer was washed with water, then concentrated and purified by column chromatography (hexane/ethyl acetate=2/1) to obtain 1.66 g (yield: 26%) of the desired product. Melting point: 177°-179° C.
21.3 g (174 mmol) of dimethylformamide dimethylacetal was dropwise added to a solution containing 33 g (145 mmol) of 4 -hydroxy-2-methyl-2H-indazole-3-sulfonamide in 200 ml of acetonitrile, at room temperature. The mixture was stirred for one hour, then poured into ice water and extracted with ethyl acetate. The organic layer was washed with water, then concentrated and purified by column chromatography to obtain 35.2 g (yield: 86.3%) of the desired product. Melting point: 118°-119° C.
4.2 g (15 mmol) of N1,N1 -dimethyl-N2 - (4-hydroxy-2-methyl-2H-indazol-3-yl)sulfonyl!formamidine was added to a suspension containing 0.6 g (15 mmol) of 60% sodium hydride in 50 ml of DMF, and the mixture was stirred at room temperature for one hour. Further, 2 g (16 mmol) of 1-bromo-2-fluoroethane was added thereto, and the mixture was stirred at room temperature for 12 hours. The mixture was poured into ice water, and the formed crystals were collected by filtration and washed with water and IPE to obtain the desired product. This product was used for the subsequent reaction without purification. Obtained amount: 3.4 g (yield: 69.5%)
A mixture comprising 3.4 g of N1,N1 -dimethyl-N2 -{ 4-(2-fluoroethoxy)-2-methyl-2H-indazol-3-yl!sulfonyl}formamidine, 5 ml of concentrated hydrochloric acid and 50 ml of ethanol, was refluxed for 12 hours. Disappearance of the starting material was confirmed by TLC, and then ethanol was distilled off. Water was added to the residue, whereupon the formed crystals were collected by filtration and washed with water and IPE to obtain 2.4 g (yield: 85%) of the desired product. Melting point: 178°-180° C.
36.1 g (0.24 mol) of 4-chloro-1H-indazole was added to a solution containing 28.4 g (0.7 mol) of sodium hydroxide in 500 ml of methanol, and 85.2 g (0.6 mol) of methyl iodide was dropwise added thereto. The mixture was heated and refluxed for 4 hours. Then, methanol was distilled off, and water was added to the residue, followed by extraction with dichloromethane. The organic layer was washed with water, dried and concentrated to obtain a mixture of 4-chloro-1-methyl-1H-indazole and 4-chloro-2-methyl-2H-indazole. This mixture was separated by silica gel column chromatography (ethyl acetate/hexane=4/1) to obtain 17.4 g (yield: 43.6%) of 4-chloro-2-methyl-2H-indazole (yellow liquid, refractive index (20° C.): 1.6095).
A solution containing 16 g (0.1 mol) of 4-chloro-2-methyl-2H-indazole in 300 ml of ethyl ether, was cooled to -30° C., and 85.4 g (0.2 mol) of n-butyl lithium (15% hexane solution) was dropwise added thereto. The mixture was stirred for one hour at the same temperature. Then, an excess amount of sulfurous acid gas was blown thereinto at a temperature of not higher than -20° C. for 3 hours. After completion of the reaction, the mixture was returned to room temperature and diluted with ethyl ether, and the product was subjected to filtration. Crystals were dried to obtain crude lithium 4-chloro-2-methyl-2H-indazole-3-sulfinate. This product was used for the subsequent reaction without purification.
45.2 g (0.4 mol) of hydroxylamine-O-sulfonic acid was gradually added to a solution containing 16 g (0.4 mol) of sodium hydroxide in water (300 ml) under cooling with ice (<10° C.). This solution was added all at once to a solution of the previously prepared crude lithium 4-chloro-2-methyl-2H-indazole-3-sulfinate in water (100 ml). The mixture was stirred at room temperature for 12 hours. Formed crystals were collected by filtration to obtain 17.1 g (yield: 69.8%) of the desired 4-chloro-2-methyl-2H-indazole-3-sulfonamide (slightly yellow granular crystals). Melting point: 173°-175° C.
0.5 g (3.3 mmol) of DBU was added to a solution containing 0.8 g (3.3 mmol) of 4-chloro-2-methyl-2H-indazole-3-sulfonamide obtained in Preparation Example 11 and 0.9 g (3.3 mmol) of phenyl (4,6-dimethoxypyrimidin-2-yl)carbamate in acetonitrile (50 ml), and the mixture was stirred at room temperature for 12 hours. The mixture was poured into ice water and acidified with citric acid. Formed crystals were collected by filtration and sequentially washed with water, isopropyl ether and ethyl ether, to obtain 1.2 g (yield: 85%) of the desired product (colorless needle-like crystals). Melting point: 171°-172° C.
The herbicide of the present invention contains an indazolesulfonylurea derivative represented by the general formula I! or II! as an active ingredient.
For the compound of the present invention to be used as a herbicide, the compound of the present invention may be used by itself. However, it may be used in the form of a formulation such as a dust, a wettable powder, an emulsifiable concentrate, a microgranule or a granule by blending it with a carrier, a surfactant, a dispersant or an adjuvant which is commonly used for formulations.
The carrier to be used for such formulations, may, for example, be a solid carrier such as Zeeklite, talc, bentonite, clay, kaolin, diatomaceous earth, fine silica, vermiculite, calcium carbonate, slaked lime, silica sand, ammonium sulfate or urea, or a liquid carrier such as isopropyl alcohol, xylene, cyclohexane or methylnaphthalene.
As the surfactant and dispersant, a metal salt of alkylbenzenesulfonic acid, a metal salt of dinaphthylmethane disulfonic acid, a salt of alcohol-sulfuric acid ester, an alkylaryl sulfonate, a lignin sulfonate, a polyoxyethylene glycol ether, a polyoxyethylene alkylaryl ether or a polyoxyethylene sorbitol monoalkylate may, for example, be mentioned.
The adjuvant may, for example, be carboxymethyl cellulose, polyethylene glycol or gum arabic.
In practical use, the herbicide may be diluted to a suitable concentration before application, or may be directly applied.
The herbicide of the present invention may be used for application to foliage, soil or water surface. The blending proportion of the active ingredient is suitably selected as the case requires. However, in a case of a dust or a granule, the proportion of the active ingredient is selected suitably within a range of from 0.01 to 10% (by weight), preferably from 0.05 to 5% (by weight). In a case of an emulsifiable concentrate or a wettable powder, the proportion is selected suitably within a range of from 1 to 50% (by weight), preferably from 5 to 30% (by weight).
The dose of the herbicide of the present invention varies depending upon the type of the compound, the weeds to be controlled, the germination tendency, the environmental conditions and the type of the formulation to be used. However, in the case of a dust or a granule which is used by itself, the dose of the active ingredient is selected suitably within a range of from 0.1 g to 5 kg, preferably from 1 g to 1 kg, per 10 ares. In a case of an emulsifiable concentrate or a wettable powder which is used in a liquid state, the dose of the active ingredient is selected suitably within a range of from 0.1 to 50,000 ppm, preferably from 10 to 10,000 ppm.
Further, the compound of the present invention may be used in combination with an insecticide, a fungicide, other herbicide, a plant growth controlling agent, a fertilizer or the like, as the case requires.
Now, the formulation method will be described with reference to typical Formulation Examples. The compounds, types of the additives and blending ratios are not limited to such specific Examples and may be changed within wide ranges. In the following description, "parts" means "parts by weight".
To 10 parts of Compound No. I-9 or II-26, 0.5 part of polyoxyethyleneoctylphenyl ether, 0.5 part of sodium β-naphthalene sulfonate-formalin condensate, 20 parts of diatomaceous earth and 69 parts of clay were mixed and pulverized to obtain a wettable powder.
To 10 parts of Compound No. I-63 or II-134, 0.5 part of polyoxyethyleneoctylphenyl ether, 0.5 part of sodium β-naphthalene sulfonate-formalin condensate, 20 parts of diatomaceous earth, 5 parts of fine silica and 64 parts of clay were mixed and pulverized to obtain a wettable powder.
To 10 parts of Compound No. I-134 or II-104, 0.5 part of polyoxyethyleneoctylphenyl ether, 0.5 part of sodium β-naphthalene sulfonate-formalin condensate, 20 parts of diatomaceous earth, 5 parts of fine silica and 64 parts of calcium carbonate, were mixed and pulverized to obtain a wettable powder.
To parts of Compound No. I-92 or II-64, 60 parts of a mixture comprising equal amounts of xylene and isophorone and 10 parts of a mixture comprising a polyoxyethylene sorbitol alkylate surfactant, a polyoxyethylenealkylaryl polymer and an alkylaryl sulfonate, were added, and the mixture was thoroughly stirred to obtain an emulsifiable concentrate.
10 Parts of Compound No. I-64 or II-142, 80 parts of a bulking agent comprising a 1:3 mixture of talc and bentonite, 5 parts of fine silica, 5 parts of a mixture comprising a polyoxyethylene sorbitol alkylate surfactant, a polyoxyethylenealkylaryl polymer and an alkylaryl sulfonate and 10 parts of water were mixed and thoroughly kneaded to obtain a paste, which was extruded from sieve apertures with a diameter of 0.7 mm. The extruded product was dried and then cut into a length of from 0.5 to 1 mm to obtain granules.
The compound of the present invention represented by the general formula I! or II! is capable of controlling annual weeds such as barnyardgrass (Echinochloa oryzicola), smallflower umbrella-plant (Cyperus difformis) and monochoria (Monochoria vaginalis) as well as perennial weeds such as Japanese ribbon wapato (Sagittaria pygmaea), arrowhead (Sagittaria trifolia), water nutgrass (Cvperus serotinus), water chestnut (Eleocharis kuroquwai), bulrush (Scirpus juncoides) and narrow-leaved arrowhead (Alisma canaliculatum), which germinate in paddy fields. Further, it exhibits excellent herbicidal effects against various weeds problematic in upland fields, including broadleaf weeds such as smartweed (Polygonum lapathifolium), green amaranth (Amaranthus viridis), lambsquater (Chenopodium album), goose grass (Galium aparine), chickweed (Stellaria media), velvetleaf (Abtilon theophrasti), prickly sida (Sida spinosa), hemp sesbania (Sesbania exaltata), morningglory (Ipomoea spp) and common cocklebur (Xanthium strumarium), perennial and annual syperaceous weeds such as purple nutsedge (Cyperus rotundus), yellow nutsedge (Cyperus esculentus), himekugu (Cyperus brevifolius var. leiolepis), annual sedge (Cyperus microiria) and rice flatsedge (Cyperus iria), and gramineous weeds such as barnyardgrass (Echinochloa crus-galli), goosegrass (Eleusine indica), greenfoxtail (Setaria viridis), annual bluegrass (Poa annua), johnsongrass (Sorghum halepense), water foxtail (Alopecurus aegualis) and wild oat (Avena fatua), over a wide range from the preemergence stage to the growing stage.
On the other hand, the herbicide of the present invention is highly safe to crop plants and exhibits particularly high safety to e.g. rice, wheat, barley, corn, grain sorghum and sugar beat.
Now, the effects of the compounds of the present invention will be described with reference to Test Examples.
In a plastic pot (surface area: 100 cm2) filled with paddy field soil, barnyardgrass (Ec), monochoria (Mo) and bulrush (Sc) were sown after puddling and leveling, and flooded to a water depth of 3 cm. Next day, a wettable powder prepared in accordance with Formulation Example 1 was diluted with water and applied dropwise to the water surface. The dose was 100 g of the active ingredient per 10 ares. The plants were then cultured in a green house, and the evaluation of the herbicidal effects was conducted on the 21st day after the application in accordance with the standards as identified in Table 4. The results are shown in Table 5.
TABLE 4
______________________________________
Herbicidal effects
Index (growth-controlling degree)
No. or phytotoxicity
______________________________________
5 Herbicidal effect or phytotoxicity:
at least 90%
4 Herbicidal effect or phytotoxicity:
at least 70% and less than 90%
3 Herbicidal effect or phytotoxicity:
at least 50% and less than 70%
2 Herbicidal effect or phytotoxicity:
at least 30% and less than 50%
1 Herbicidal effect or phytotoxicity:
at least 10 and less than 30%
0 Herbicidal effect or phytotoxicity:
0 to less than 10%
______________________________________
TABLE 5
______________________________________
Herbicidal
Compound effects
No. Ec Mo Sc
______________________________________
I-5 5 5 5
I-6 5 5 5
I-8 5 5 5
I-17 5 5 5
I-18 5 5 5
I-19 5 5 5
I-20 5 5 5
I-23 5 5 5
I-25 5 5 5
I-26 5 5 5
I-27 5 5 5
I-28 5 5 5
I-29 5 5 5
I-31 5 5 5
I-32 5 5 5
I-33 5 5 5
I-34 5 5 5
I-35 5 5 5
I-63 5 5 5
I-64 5 5 5
I-65 5 5 5
I-66 5 5 5
I-67 5 5 5
I-79 5 5 5
I-91 5 5 5
I-92 5 5 5
I-93 5 5 5
I-94 5 5 5
I-95 5 5 5
I-111 5 5 5
I-114 5 5 5
I-120 5 5 5
I-131 5 5 5
I-134 5 5 5
I-136 3 5 5
I-149 5 5 4
I-150 5 5 5
I-151 5 5 4
I-153 5 5 5
I-157 5 5 5
I-158 5 5 5
I-160 5 5 5
I-161 5 5 5
I-162 5 5 5
I-174 5 5 5
I-175 5 5 5
I-176 5 5 5
I-179 5 5 5
I-180 5 5 5
I-181 5 5 5
I-182 5 5 5
I-183 5 5 5
I-184 5 5 5
I-194 5 5 5
I-204 5 5 5
I-205 5 5 5
I-216 5 5 5
I-218 5 5 4
I-322 5 5 5
I-334 5 5 5
I-337 5 5 5
I-506 5 5 5
I-507 5 5 5
I-508 4 5 4
I-513 5 5 5
I-514 5 5 5
I-516 5 5 5
I-517 5 5 5
I-518 5 5 5
I-519 5 5 4
I-520 3 5 5
I-527 3 5 5
I-530 5 5 5
I-555 5 5 4
I-641 5 5 5
I-645 3 5 5
I-906 3 5 5
II-5 5 5 5
II-6 5 5 5
II-8 5 5 5
II-17 5 5 5
II-18 4 5 4
II-19 5 5 5
II-20 5 5 5
II-23 5 5 5
II-25 5 5 5
II-26 5 5 5
II-27 5 5 5
II-28 5 5 5
II-29 5 5 5
II-31 5 5 5
II-32 5 5 5
II-33 5 5 5
II-34 5 5 5
II-35 5 5 5
II-36 5 5 5
II-38 5 5 5
II-42 4 5 5
II-53 5 5 5
II-55 5 5 5
II-63 5 5 5
II-64 5 5 5
II-65 5 5 5
II-66 5 5 5
II-67 5 5 5
II-91 5 5 5
II-92 5 5 5
II-93 5 5 5
II-94 5 5 5
II-95 5 5 5
II-104 5 5 5
II-106 5 5 5
II-107 5 5 5
II-110 5 5 5
II-111 5 5 5
II-112 5 5 5
II-113 5 5 5
II-114 5 5 5
II-115 5 5 5
II-120 5 5 5
II-127 5 5 5
II-129 4 5 5
II-130 5 5 5
II-131 5 5 5
II-132 3 5 5
II-134 5 5 5
II-136 3 5 5
II-137 5 5 5
II-141 5 5 5
II-142 5 5 5
II-143 5 5 5
II-149 5 5 5
II-150 5 5 5
II-151 5 5 5
II-153 5 5 5
II-155 5 5 5
II-156 5 5 5
II-157 5 5 5
II-158 5 5 5
II-159 5 5 5
II-160 5 5 5
II-161 5 5 5
II-162 5 5 5
II-163 5 5 5
II-166 5 5 5
II-168 5 5 5
II-169 5 5 5
II-174 5 5 5
II-175 5 5 5
II-176 5 5 5
II-177 5 5 5
II-178 5 5 5
II-179 5 5 5
II-180 5 5 5
II-181 5 5 5
II-182 5 5 5
II-183 5 5 5
II-184 5 5 5
II-185 5 5 5
II-188 5 5 5
II-189 5 5 5
II-194 5 5 5
II-195 5 5 5
II-197 5 5 5
II-198 5 5 5
II-199 5 5 5
II-200 5 5 5
II-202 4 5 5
II-204 5 5 5
II-208 5 5 5
II-215 5 5 5
II-220 5 5 5
II-225 5 5 5
II-227 5 5 5
II-531 5 5 5
______________________________________
In a plastic pot (surface area: 120 cm2) filled with upland field soil, pale smartweed (Po), slender amaranth (Am), common lambsquarters (Ch) and rice flatsedge (Ci) were sown and covered with soil. A wettable powder prepared in accordance with Formulation Example 1 was diluted with water and applied uniformly to the soil surface by a small-sized sprayer in an amount of 100 l/10 ares so as to apply 100 g of the active ingredient per 10 ares. The plants were then cultured in a green house, and the evaluation of the herbicidal effects was conducted on the 21st day after the application in accordance with the standards as identified in Table 4. The results are shown in Table
TABLE 6
______________________________________
Herbicidal
Compound effects
No. Po Am Ch Ci
______________________________________
I-5 5 5 5 5
I-6 5 5 5 5
I-8 5 5 5 5
I-17 5 5 5 5
I-18 5 5 5 5
I-19 5 5 5 5
I-20 5 5 5 5
I-23 5 5 5 --
I-25 5 5 5 --
I-26 5 5 5 5
I-27 5 5 5 5
I-28 5 5 5 --
I-29 5 5 5 --
I-31 5 5 5 5
I-32 5 5 5 5
I-33 5 5 5 5
I-34 5 5 5 5
I-35 5 5 5 5
I-53 5 5 5 5
I-63 5 5 5 5
I-64 5 5 5 5
I-65 5 5 5 5
I-66 5 5 5 5
I-67 5 5 5 5
I-79 5 5 5 5
I-91 5 5 5 5
I-92 5 5 5 5
I-93 5 5 5 5
I-94 5 5 5 5
I-95 5 5 5 5
I-110 5 5 5 5
I-111 5 5 5 5
I-112 5 5 5 5
I-113 5 5 5 5
I-114 5 5 5 5
I-120 5 5 5 5
I-131 5 5 5 5
I-134 5 5 5 5
I-136 5 5 5 5
I-149 5 5 5 5
I-150 5 5 5 5
I-151 5 5 5 5
I-152 5 5 4 5
I-153 5 5 5 5
I-157 5 5 5 5
I-158 5 5 5 5
I-160 5 5 5 5
I-161 5 5 5 5
I-162 5 5 5 5
I-174 5 5 5 5
I-175 5 5 5 5
I-176 5 5 5 --
I-177 5 5 5 --
I-178 5 5 5 5
I-179 5 5 5 --
I-180 5 5 5 5
I-181 5 5 5 5
I-182 5 5 5 5
I-183 5 5 4 5
I-184 5 5 4 5
I-194 5 5 5 5
I-198 5 5 5 5
I-199 5 5 5 5
I-204 5 5 5 5
I-205 5 5 4 5
I-209 5 5 4 5
I-212 5 5 5 5
I-216 5 5 5 5
I-218 4 5 4 5
I-322 5 5 5 --
I-334 5 5 5 --
I-337 5 5 5 --
I-506 5 5 5 5
I-507 5 5 5 5
I-508 5 5 5 5
I-509 5 5 4 5
I-511 5 5 5 4
I-513 5 5 5 5
I-514 5 5 5 4
I-516 5 5 5 5
I-517 4 5 4 5
I-518 5 5 5 5
I-519 5 5 5 5
I-520 5 5 5 5
I-521 5 5 5 5
I-525 5 5 5 5
I-526 4 5 4 5
I-527 5 5 5 5
I-528 5 5 5 5
I-529 4 5 5 5
I-530 5 5 5 5
I-555 5 5 5 5
I-641 5 5 5 5
I-761 4 5 4 --
I-905 5 5 5 --
I-906 5 5 5 --
II-5 5 5 5 5
II-6 5 5 4 5
II-8 5 5 5 5
II-17 5 5 5 5
II-19 5 5 5 5
II-20 5 5 5 5
II-23 5 5 5 5
II-25 5 5 4 5
II-26 5 5 5 5
II-27 5 5 5 5
II-28 5 5 5 5
II-29 5 5 5 --
II-31 5 5 5 5
II-32 5 5 5 5
II-34 5 5 5 5
II-35 5 5 5 5
II-36 5 5 5 5
II-38 5 5 4 5
II-53 5 5 5 --
II-55 5 5 4 5
II-56 5 5 5 5
II-63 5 5 5 5
II-64 5 5 5 5
II-65 5 5 5 --
II-66 5 5 5 --
II-67 5 5 5 --
II-90 4 5 5 --
II-91 5 5 5 5
II-92 5 5 5 5
II-93 5 5 4 5
II-95 4 5 4 5
II-96 5 5 4 5
II-104 5 5 5 --
II-105 4 5 5 --
II-106 5 5 5 5
II-107 5 5 5 5
II-110 5 5 5 5
II-111 5 5 5 5
II-113 5 5 5 5
II-114 5 5 5 5
II-115 5 5 4 4
II-120 5 5 5 5
II-127 5 5 5 5
II-130 5 5 4 5
II-131 5 5 5 5
II-134 5 5 5 5
II-136 5 5 5 5
II-137 5 5 5 --
II-138 5 5 5 --
II-139 5 5 5 --
II-140 5 5 4 --
II-141 5 5 5 --
II-142 5 5 5 --
II-143 5 5 5 --
II-144 5 5 5 --
II-145 5 5 5 --
II-146 5 5 5 5
II-149 5 5 4 5
II-150 5 5 5 5
II-155 5 5 5 5
II-156 4 5 5 5
II-157 5 5 5 5
II-158 5 5 5 5
II-160 5 5 5 5
II-161 4 5 4 5
II-162 5 5 5 5
II-163 5 5 4 5
II-164 5 5 5 5
II-166 5 5 5 5
II-167 4 5 5 5
II-168 5 5 5 5
II-169 5 5 5 5
II-170 4 5 5 5
II-172 5 5 5 5
II-174 5 5 5 5
II-175 5 5 5 --
II-176 5 5 5 --
II-177 5 5 5 --
II-178 5 5 5 --
II-179 5 5 5 --
II-180 5 5 5 5
II-181 5 5 5 5
II-182 5 5 5 5
II-183 5 5 4 5
II-184 5 5 5 5
II-185 5 5 5 --
II-188 5 5 5 5
II-189 5 5 5 5
II-191 5 5 5 --
II-195 5 5 5 4
II-197 5 5 5 --
II-198 5 5 5 --
II-199 5 5 5 --
II-200 5 5 5 --
II-204 5 5 4 5
II-207 5 5 4 --
II-219 4 5 5 5
II-220 5 5 5 --
II-223 5 5 5 --
II-225 5 5 5 5
II-226 5 5 5 5
II-227 5 5 5 --
II-531 5 5 5 --
______________________________________
In a plastic pot (surface area: 120 cm2) filled with upland field soil, pale smartweed (Po), slender amaranth (Am), common lambsquarters (Ch) and rice flatsedge (Ci) were sown and covered with soil and were cultured in a green house for 2 weeks. A wettable powder prepared in accordance with Formulation Example 1 was diluted with water and applied onto the entire foliages of the plants from above by a small-sized sprayer in an amount of 100 l/10 ares so as to apply 100 g of the active ingredient per 10 ares. The plants were then cultured in the green house, and the evaluation of the herbicidal effects was conducted on the 14th day after the treatment in accordance with the standards as identified in Table 4. The results are shown in Table 7.
TABLE 7
______________________________________
Herbicidal
Compound effects
No. Po Am Ch Ci
______________________________________
I-5 5 5 5 5
I-6 5 5 5 5
I-8 5 5 5 5
I-17 5 5 5 5
I-18 5 5 5 5
I-19 5 5 5 5
I-20 5 5 5 5
I-23 5 5 5 5
I-25 5 5 5 5
I-26 5 5 5 5
I-27 5 5 5 5
I-28 5 5 5 5
I-29 5 5 5 5
I-31 5 5 5 5
I-32 5 5 5 5
I-33 5 5 5 5
I-34 5 5 5 5
I-35 5 5 5 5
I-53 5 5 5 5
I-63 5 5 5 5
I-64 5 5 5 5
I-65 5 5 5 5
I-66 5 5 5 5
I-67 5 5 5 5
I-79 5 5 5 5
I-91 5 5 5 5
I-92 5 5 5 5
I-93 5 5 5 5
I-94 5 5 5 5
I-95 5 5 5 5
I-111 5 5 5 5
I-112 5 5 5 5
I-113 5 5 5 5
I-114 5 5 5 5
I-120 5 5 5 5
I-131 5 5 5 5
I-134 5 5 5 5
I-136 5 5 4 4
I-149 4 5 4 5
I-150 5 5 5 5
I-151 5 5 5 5
I-157 5 5 5 5
I-158 5 5 5 5
I-160 5 5 5 5
I-161 5 5 5 5
I-162 5 5 5 5
I-174 5 5 5 5
I-175 5 5 5 5
I-176 5 5 5 5
I-177 4 4 5 5
I-178 5 5 5 5
I-179 5 5 5 5
I-180 5 5 5 5
I-181 5 5 5 5
I-182 5 5 5 5
I-183 5 5 5 4
I-184 5 5 5 5
I-194 5 5 5 5
I-204 5 5 5 5
I-205 5 5 5 5
I-206 5 5 5 4
I-209 4 5 5 4
I-211 4 5 5 4
I-212 4 5 5 4
I-216 5 5 5 5
I-218 5 5 4 4
I-322 5 5 5 5
I-324 4 5 4 5
I-334 5 5 4 5
I-337 5 5 5 5
I-506 4 5 4 5
I-507 5 5 5 5
I-508 5 5 5 5
I-509 5 5 5 5
I-511 4 5 5 4
I-513 5 5 5 5
I-514 5 5 5 4
I-516 5 5 5 5
I-517 5 5 4 5
I-518 5 5 5 5
I-520 5 5 5 5
I-525 5 5 5 5
I-526 5 5 5 4
I-527 5 5 5 5
I-528 5 5 5 5
I-530 5 5 5 5
I-555 5 5 5 5
I-641 5 5 5 5
II-5 5 5 5 5
II-6 4 5 5 5
II-8 5 5 4 5
II-17 5 5 4 5
II-19 5 5 5 5
II-20 5 5 5 5
II-23 5 5 5 5
II-25 5 5 5 5
II-26 5 5 5 5
II-27 5 5 5 5
II-28 5 5 5 5
II-29 5 5 5 5
II-31 5 5 4 5
II-32 5 5 5 5
II-34 5 5 5 5
II-35 5 5 5 5
II-38 5 5 4 5
II-53 5 5 5 5
II-55 5 5 5 5
II-56 5 5 5 5
II-63 5 5 5 5
II-64 5 5 5 5
II-65 5 5 5 5
II-66 5 5 5 5
II-67 5 5 5 5
II-91 5 5 5 5
II-92 5 5 5 5
II-93 5 5 5 5
II-94 5 5 5 5
II-104 5 5 5 5
II-105 5 5 5 5
II-106 5 5 5 5
II-107 5 5 5 5
II-110 5 5 5 5
II-111 5 5 5 5
II-112 5 5 5 5
II-113 5 5 5 5
II-114 5 5 5 5
II-115 5 5 4 5
II-120 5 5 5 5
II-129 5 5 5 5
II-130 5 5 5 5
II-131 5 5 5 5
II-134 5 5 5 5
II-136 5 5 4 4
II-140 5 5 5 5
II-141 4 5 4 5
II-142 5 5 5 5
II-143 5 5 5 5
II-146 5 5 4 5
II-149 5 5 5 5
II-150 5 5 5 5
II-153 5 5 4 4
II-154 5 5 5 4
II-155 5 5 5 5
II-157 5 5 5 5
II-158 5 5 4 5
II-160 5 5 5 5
II-162 5 5 5 5
II-166 5 5 5 5
II-167 5 5 5 5
II-168 5 5 5 5
II-169 5 5 5 5
II-170 4 5 5 5
II-174 5 5 4 5
II-175 5 5 4 5
II-176 5 4 5 5
II-178 5 5 5 5
II-179 5 5 5 5
II-180 5 5 5 5
II-181 5 5 5 5
II-182 5 5 5 5
II-183 5 5 4 5
II-184 5 5 5 5
II-188 5 5 5 5
II-189 5 5 4 5
II-192 4 5 4 5
II-194 5 5 5 5
II-195 5 5 5 5
II-196 4 5 4 5
II-197 5 5 5 5
II-199 5 5 5 5
II-204 5 5 5 5
II-218 5 5 5 4
II-219 4 5 5 4
II-220 5 5 4 5
II-225 5 5 5 5
II-226 5 5 5 5
II-531 5 5 5 5
______________________________________
In a 1/10,000a plastic pot, paddy field soil was filled, irrigated, paddled and leveled. Then, barnyardgrass (Ec), monochoria (Mo) and bulrush (Sc) were sown at a depth of 0.5 cm. Further, two seedlings of rice (Or) of 2 leaf stage was transplanted at a transplantation depth of 2 cm. Then, the pot was flooded to a water depth of 3 cm. Next day, a prescribed amount of the active ingredient (gai /10a) of a wettable powder prepared in accordance with Formulation Example 1 was diluted with water and applied dropwise to the water surface. The plants were then cultured in a green house, and the evaluation of the herbicidal effects and phytotoxicity was conducted on the 28th day after the application in accordance with the standards as identified in Table 4. The results are shown in Table 8.
TABLE 8
______________________________________
Herbicidal Phytoto-
Compound Dose effects xicity
No. (gai 10a) Eo Mo Sc Or
______________________________________
I-17 25 4 5 5 0
I-157 6.3 5 5 5 1
I-161 25 5 5 5 0
I-174 25 5 5 4 1
I-216 25 4 5 4 2
II-19 25 5 5 5 0
6.3 5 5 5 0
II-23 25 4 5 5 0
II-26 25 5 5 5 1
6.3 5 5 5 0
1.6 5 5 4 0
II-27 25 5 5 5 0
6.3 5 5 5 0
II-29 6.3 5 5 5 1
1.6 3 5 5 0
II-31 6.3 5 5 5 1
1.6 5 5 5 0
II-35 25 5 5 5 1
6.3 5 5 5 0
II-36 25 5 5 5 0
II-53 25 5 5 5 0
II-64 25 5 5 5 0
6.3 5 5 5 0
II-65 25 5 5 5 0
6.3 5 5 5 0
II-66 25 5 5 5 1
6.3 S 5 5 0
II-92 25 5 5 5 2
6.3 5 5 5 0
1.6 5 5 5 0
II-93 25 5 5 5 1
6.3 5 5 5 0
II-94 25 5 5 5 1
6.3 5 5 5 0
II-104 25 5 5 5 0
6.3 5 5 5 0
II-114 6.3 5 5 5 1
1.6 5 5 5 0
II-127 25 5 5 5 1
6.3 3 5 5 0
II-134 25 5 5 5 0
6.3 5 5 5 0
II-137 25 5 5 5 2
6.3 5 5 5 0
1.6 5 5 5 0
II-141 25 5 5 5 1
6.3 5 5 4 0
II-142 6.3 5 5 5 0
1.6 5 5 5 0
II-157 25 5 5 5 0
6.3 5 5 5 0
II-160 25 5 5 5 0
6.3 5 5 5 0
II-162 25 5 5 5 1
6.3 5 5 5 0
II-166 1.6 5 5 5 0
II-178 25 5 5 5 0
6.3 4 5 4 0
II-208 25 5 5 5 0
6.3 4 5 4 0
II-531 25 5 5 5 0
6.3 5 5 4 0
Compara- 25 5 5 5 5
tive 6.3 5 5 4 5
compound 1.6 3 4 2 5
______________________________________
Comparative compound A: Disclosed in Japanese Unexamined Patent
Publication No. 95091/1992 (Compound No. 1)
In a plastic pot (surface area: 600 cm2) filled with upland field soil, seeds or tubers of wheat (Tr), corn (Ze), grain sorghum (Gs), pale smartweed (Po), slender amaranth (Am), common lambsquarters (Ch), velvetleaf (Ab), morningglory (Ip), cocklebur (Xa) and purple nutsedge (CR) were planted and covered with soil. Next day, a prescribed amount of the active ingredient (gai /10a) of a wettable powder prepared in accordance with Formulation Example 1 was diluted with water and applied uniformly to the soil surface by a small-sized sprayer in an amount of 100 l per 10 ares. The plants were then cultured in a green house, and the evaluation of the herbicidal effects was conducted on the 21st day after the application in accordance with the standards as identified in Table 4. The results are shown in Table 9.
TABLE 9
______________________________________
Com- Herbicidal Phytoto-
pound Dose effects xicity
No. (gai 10a)
Po Am Ch Ab Ip Xa CR Tr Ze Gs
______________________________________
II-19 25 5 5 5 5 5 5 2 0 1 0
II-23 25 5 5 5 5 5 5 5 0 3 1
6.3 4 5 4 5 4 5 5 0 3 0
II-26 25 5 5 5 5 5 5 -- 1 4 3
6.3 5 5 4 4 4 4 4 0 3 1
II-28 25 5 5 5 5 5 5 -- 0 1 0
6.3 5 5 4 4 4 4 4 0 0 0
II-29 25 5 5 5 5 5 5 5 0 3 3
6.3 5 5 5 5 5 5 5 0 1 1
II-35 6.3 5 5 5 4 4 4 5 0 1 0
II-53 25 5 5 5 5 5 5 5 1 2 1
6.3 5 5 5 5 5 5 4 0 0 0
II-63 25 5 5 5 5 5 5 5 0 5 3
6.3 5 5 5 5 5 5 5 0 3 2
II-64 6.3 5 5 5 5 5 5 5 0 1 3
1.6 5 5 5 3 5 5 5 0 0 0
II-65 25 5 5 5 5 5 5 5 1 1 4
6.3 5 5 5 4 4 5 5 0 0 3
II-66 25 5 5 5 5 5 5 5 0 4 4
6.3 5 5 5 5 4 5 5 0 1 3
II-91 6.3 5 5 5 5 5 5 5 0 4 1
II-104 25 5 5 5 5 5 5 5 0 4 3
6.3 5 5 5 4 4 5 5 0 1 3
II-107 25 5 5 5 5 5 5 5 0 4 4
6.3 5 5 5 4 3 5 5 0 3 3
II-134 25 5 5 5 5 5 5 5 1 1 1
6.3 5 5 5 5 5 5 5 0 0 0
II-137 25 5 5 5 5 5 5 5 0 4 2
6.3 5 5 5 5 4 5 5 0 3 1
II-142 25 5 5 5 5 5 5 5 1 4 4
6.3 5 5 5 5 5 5 5 0 3 3
II-157 25 5 5 5 5 5 5 4 2 4 0
6.3 5 5 5 5 3 5 3 0 1 0
II-168 25 5 5 5 5 5 5 4 1 4 4
6.3 5 5 5 4 4 5 3 0 3 3
II-215 25 5 5 5 4 5 5 5 1 2 1
______________________________________
In a plastic pot (surface area: 600 cm2) filled with upland field soil, seeds or tubers of wheat (Tr), corn (Ze), grain sorghum (Gs), pale smartweed (Po), slender amaranth (Am), common lambsquarters (Ch), velvetleaf (Ab), morningglory (Ip), cocklebur (Xa) and purple nutsedge (CR) were planted, covered with soil and cultured in a green house for 2 weeks. Then, a prescribed amount of the active ingredient (gai /10a) of a wettable powder prepared in accordance with Formulation Example 1 was diluted with water and applied onto the entire foliages of the plants from above by a small-sized sprayer in an amount of 100 l per 10 ares. The plants were then cultured in a green house, and the evaluation of the herbicidal effects was conducted on the 14th day after the treatment in accordance with the standards as identified in Table 4. The results are shown in Table 10.
TABLE 10
______________________________________
Com- Herbicidal Phytotox-
pound Dose effects icity
No. (gai 10 a)
Po Am Ch Ab Ip Xa CR Tr Ze Gs
______________________________________
I-20 6.3 5 5 5 5 5 5 3 1 3 3
I-23 25 5 5 5 5 5 5 2 0 4 3
6.3 5 5 5 5 5 5 0 0 3 3
I-26 1.6 5 5 5 5 5 5 5 1 4 4
I-27 6.3 5 5 5 5 5 5 3 1 3 3
1.6 5 5 4 5 5 5 1 0 3 3
I-28 25 5 5 5 5 5 5 2 1 3 3
6.3 5 5 4 5 4 5 1 0 3 3
I-53 25 5 5 5 5 5 5 3 1 3 3
6.3 5 5 5 5 5 5 1 0 3 2
I-66 6.3 5 5 5 5 5 5 2 1 3 --
I-176 25 5 5 5 5 5 5 3 1 3 3
6.3 5 5 5 5 5 4 2 0 3 3
I-194 25 5 5 4 5 5 5 3 0 4 4
I-204 25 5 5 4 5 5 5 -- 1 4 4
6.3 4 5 4 5 5 5 -- 0 4 3
I-337 25 5 5 5 5 5 5 4 1 4 3
6.3 4 5 5 5 5 5 4 0 3 3
I-516 25 4 5 5 5 5 5 2 0 4 3
II-20 25 5 5 5 5 5 5 5 0 4 3
6.3 5 5 5 5 5 5 5 0 4 3
II-26 25 5 5 5 5 5 5 5 0 3 1
6.3 5 5 5 5 5 5 5 0 2 1
II-27 25 5 5 5 5 5 5 2 0 0 0
6.3 5 5 5 5 5 5 1 0 0 0
II-28 25 5 5 5 5 5 5 -- 1 3 3
6.3 5 5 5 5 5 5 5 0 2 2
II-31 25 5 5 5 5 5 5 5 1 1 1
6.3 5 5 4 5 5 5 5 0 1 1
II-64 25 5 5 5 5 5 5 4 0 0 3
6.3 5 5 5 5 5 5 4 0 0 2
II-93 25 5 5 5 5 5 5 5 1 1 3
6.3 5 5 5 5 5 5 5 0 1 3
II-104
100 5 5 5 5 5 5 5 0 0 3
25 5 5 5 5 5 5 4 0 0 3
II-127
25 5 5 4 5 5 5 5 0 4 1
II-134
25 5 5 5 5 5 5 5 0 0 0
6.3 5 5 4 5 5 5 5 0 0 0
II-150
25 5 5 4 5 5 5 -- 0 1 3
II-157
25 5 5 5 5 5 5 -- 0 0 2
6.3 5 5 4 5 5 5 -- 0 0 1
II-168
25 5 5 5 5 5 5 4 1 4 3
6.3 5 5 4 5 5 5 3 0 2 3
II-180
25 5 5 5 5 5 5 -- 0 0 1
6.3 5 5 4 5 5 5 -- 0 0 1
II-181
25 5 5 5 5 5 5 5 1 3 2
6.3 5 5 5 5 5 5 4 0 1 1
______________________________________
Claims (2)
1. An indazolesulfonamide derivative represented by the formula: ##STR79## wherein R1 is a hydrogen atom, a C1-30 -alkyl group, a C3-7 -cycloalkyl group, a halo-C1-30 -alkyl group, a C1-30 -alkoxy-C1-30 -alkyl group, a benzyloxy-C1-30 -alkyl group, a benzyl group, a phenyl group, a pyridyl group, a di-C1-30 -alkylaminocarbonyl group, a C1-30 -alkoxycarbonyl group, a C1-30 -alkylsulfonyl group, a phenylsulfonyl group, a di-C1-30 -alkylaminosulfonyl group, a halo-C1-30 -alkylcarbonyl group, a C1-30 -alkylcarbonyl group, a benzoyl group or a C2-20 -alkenyl group, R2 and R3 are the same or different and represent a hydrogen atom, a halogen atom, a C1-30 -alkyl group, a C3-7 -cycloalkyl group, a C2-20 -alkenyl group, a C1-30 -alkoxycarbonyl-C2-20 -alkenyl group, a C2-20 -alkynyl group, a halo-C1-30 -alkyl group, a C1-30 -alkoxy-C1-30 -alkyl group, a C1-30 -alkoxycarbonyl-C1-30 -alkyl group, a C1-30 -alkylcarbonyl-C1-30 -alkyl group, a C3-7 -cycloalkylcarbonyl-C1-30 -alkyl group, a cyano-C1-30 -alkyl group, a di-C1-30 -alkylaminocarbonyl-C1-30 -alkyl group, a di-C1-30 -alkylamino-C1-30 -alkyl group, a di-C1-30 -alkylaminosulfonyl-C1-30 -alkyl group, an azido-C1-30 -alkyl group, a benzyl group, a phenyl group, a nitro group, a cyano group, an azide group, an amino group, a mono C1-30 -alkylamino group, a di-C1-30 -alkylamino group, a benzylamino group, a C1-30 -alkylcarbonylamino group which optionally is substituted by a halogen atom, a benzoylamino group, a C1-30 -alkoxycarbonylamino group, a phenoxycarbonylamino group, a C1-30 -alkylsulfonylamino group wherein the amino group optionally is substituted by a C1-30 -alkyl group, a phenylsulfonylamino group wherein the amino group optionally is substituted by a C1-30 -alkyl group, a C1-30 -alkylideneamino group, a benzylideneamino group, a tetrazolyl group which optionally is substituted by a methyl group, a group represented by the formula --COR4 wherein R4 is a hydrogen atom, a hydroxyl group, a C1-30 -alkyl group, a C3-7 -cycloalkyl group, a halo-C1-30 -alkyl group, a C2-20 -alkenyl group, a C2-20 -alkynyl group, a benzyl group, a phenyl group, a C1-30 -alkoxy group, a halo-C1-30 -alkoxy group, a C1-30 -alkoxy-C1-30 - alkoxy group, a C2-20 -alkenyloxy group, a halo-C2-20 -alkenyloxy group, a C2-20 -alkynyloxy group, a benzyloxy group or a phenoxy group; a group represented by the formula --C(O)NR5 R6 wherein R5 and R6 are the same or different and represent a hydrogen atom, a C1-30 -alkyl group, a C2-20 -alkenyl group, a C2-20 -alkynyl group, a benzyl group, a phenyl group or a C1-30 -alkoxy group; a group represented by the formula --SR7 wherein R7 is a hydrogen atom, a C1-30 -alkyl group or a halo-C1-30 -alkyl group; a group represented by the formula --So2 NR5 R6, wherein R5 and R6 have the same meanings as defined above; a group represented by the formula --S(O)n R8, wherein n represents an integer of 1 or 2, and R8 represents a C1-30 -alkyl group, a C2-20 -alkenyl group or a halo-C1-30 -alkyl group; a group represented by the formula --OR9, wherein R9 is a hydrogen atom, a C1-30 -alkyl group, a C3-7 -cycloalkyl C1-30 -alkyl group, a C2-20 -alkenyl group, a C2-20 -alkynyl group, a benzyl group optionally substituted by a halogen atom, a C1-30 -alkyl group or a C1-30 -alkoxy group; a halo-C1-30 -alkyl group, a halo-C2-20 -alkenyl group, a phenyl group optionally substituted by a halogen atom, a C1-30 -alkyl group or a C1-30 -alkoxy group; a C1-30 -alkoxy-C1-30 -alkyl group, a C1-30 -alkoxy-C1-30 -alkoxy-C1-30 -alkyl group, a halo-C1-30 -alkoxy-C1-30 -alkyl group, a benzyloxy-C1-30 -alkyl group, a phenoxy-C1-30 -alkyl group, a C1-30 -alkylthio-C1-30 -alkyl group, a di-C1-30 -alkylamino-C1-30 -alkyl group, an azido C1-30 -alkyl group, a C1-30 -alkylcarbonyl group, a halo-C1-30 -alkylcarbonyl group, a benzoyl group, a di-C1-30 -alkylaminocarbonyl group, a cyano-C1-30 -alkyl group, a C1-30 -alkylideneamino group, a di-C1-30 -alkylideneamino group, a benzylideneamino group or a C1-30 -alkoxycarbonyl-C1-30 -alkyl group; or the formula --C(═NOR10)R11, wherein R10 represents a hydrogen atom, a C1-30 -alkyl group, a C2-20 -alkenyl group, a C2-20 -alkynyl group, a benzyl group, a halo-C1-30 -alkyl group or a phenyl group, and R11 represents a hydrogen atom, a C1-30 -alkyl group, a benzyl group, a halo-C1-30 -alkyl group or a phenyl group, and R2 and R3 together may form a --OC2 H4 O--, --SC2 H4 S-- or --OCH2 -- group.
2. An indazolesulfonamide derivative represented by the formula: ##STR80## wherein R1 is a hydrogen atom, a C1-30 -alkyl group, a C3-7 -cycloalkyl group, a halo-C1-30 -alkyl group, a C1-30 -alkoxy-C1-30 -alkyl group, a benzyloxy-C1-30 -alkyl group, a benzyl group, a phenyl group, a pyridyl group, a di-C1-30 -alkylaminocarbonyl group, a C1-30 -alkoxycarbonyl group, a C1-30 -alkylsulfonyl group, a phenylsulfonyl group, a di-C1-30 -alkylaminosulfonyl group, a halo-C1-30 -alkylcarbonyl group, a C1-30 -alkylcarbonyl group, a benzoyl group or a C2-20 -alkenyl group, R2 and R3 are the same or different and represent a hydrogen atom, a halogen atom, a C1-30 -alkyl group, a C3-7 -cycloalkyl group, a C2-20 -alkenyl group, a C1-30 -alkoxycarbonyl-C2-20 -alkenyl group, a C2-20 -alkynyl group, a halo-C1-30 -alkyl group, a C1-30 -alkoxy-C1-30 -alkyl group, a C1-30 - alkoxycarbonyl-C1-30 -alkyl group, a C1-30 -alkylcarbonyl-C1-30 -alkyl group, a C3-7 -cycloalkylcarbonyl-C1-30 -alkyl group, a cyano-C1-30 -alkyl group, a di-C1-30 -alkylaminocarbonyl-C1-30 -alkyl group, a di-C1-30 alkylamino-C1-30 -alkyl group, a di-C1-30 -alkylaminosulfonyl-C1-30 -alkyl group, an azido-C1-30 -alkyl group, a benzyl group, a phenyl group, a nitro group, a cyano group, an azide group, an amino group, a mono-C1-30 -alkylamino group, a di-C1-30 -alkylamino group, a benzylamino group, a C1-30 -alkylcarbonylamino group which optionally is substituted by a halogen atom, a benzoylamino group, a C1-30 -alkoxycarbonylamino group, a phenoxycarbonylamino group, a C1-30 -alkylsulfonylamino group wherein the amino group optionally is substituted by a C1-30 -alkyl group, a phenylsulfonylamino group wherein the amino group optionally is substituted by a C1-30 -alkyl group, a C1-30 -alkylideneamino group, a benzylideneamino group, a tetrazolyl group which optionally is substituted by a methyl group, a group represented by the formula --COR4, wherein R4 is a hydrogen atom, a hydroxyl group, a C1-30 -alkyl group, a C3-7 -cycloalkyl group, a halo-C1-30 -alkyl group, a C2-20 -alkenyl group, a C2-20 -alkynyl group, a benzyl group, a phenyl group, a C1-30 -alkoxy group, a halo-C1-30 -alkoxy group, a C1-30 -alkoxy-C1-30 - alkoxy group, a C2-20 -alkenyloxy group, a halo-C2-20 -alkenyloxy group, a C2-20 -alkynyloxy group, a benzyloxy group or a phenyloxy group; a group represented by the formula --C(O)NR5 R6, wherein R5 and R6 are the same or different and represent a hydrogen atom, a C1-30 -alkyl group, a C2-20 -alkenyl group, a C2-20 - alkynyl group, a benzyl group, a phenyl group or a C1-30 -alkoxy group; a group represented by the formula --SR7, wherein R7 is a hydrogen atom, a C1-30 -alkyl group or a halo-C1-30 -alkyl group; a group represented by the formula --SO2 NR5 R6, wherein R5 and R6 have the same meanings as defined above; a group represented by the formula --S(O)n R8, wherein n represents an integer of 1 or 2, and R8 represents a C1-30 -alkyl group, a C2-20 -alkenyl group or a halo-C1-30 -alkyl group; a group represented by the formula --OR9, wherein R9 is a hydrogen atom, a C1-30 -alkyl group, a C3-7 -cycloalkyl-C1-30 -alkyl group, a C2-20 -alkenyl group, a C2-20 - alkynyl group, a benzyl group optionally substituted by a halogen atom, a C1-30 -alkyl group or a C1-30 -alkoxy group; a halo-C1-30 -alkyl group, a halo-C2-20 -alkenyl group, a phenyl group optionally substituted by a halogen atom, a C1-30 -alkyl group or a C1-30 -alkoxy group; a C1-30 -alkoxy-C1-30 -alkyl group, a C1-30 -alkoxy-C1-30 -alkoxy-C1-30 -alkyl group, a halo-C1-30 -alkoxy-C1-30 -alkyl group, a benzyloxy-C1-30 -alkyl group, a phenoxy-C1-30 - alkyl group, a C1-30 -alkylthio-C1-30 -alkyl group, a di-C1-30 -alkylamino-C1-30 -alkyl group, an azido-C1-30 -alkyl group, a C1-30 -alkylcarbonyl group, a halo-C1-30 -alkylcarbonyl group, a benzoyl group, a di-C1-30 -alkylaminocarbonyl group, a cyano-C1-30 -alkyl group, a C1-30 -alkylideneamino group, a di-C1-30 -alkylideneamino group, a benzylideneamino group or a C1-30 -alkoxycarbonyl-C1-30 -alkyl group, or the formula --C(═NOR10)R11, wherein R10 represents a hydrogen atom, a C1-30 -alkyl group, a C2-20 -alkenyl group, a C2-20 -alkynyl group, a benzyl group, a halo-C1-30 -alkyl group or a phenyl group, and R11 represents a hydrogen atom, a C1-30 -alkyl group, a benzyl group, a halo-C1-30 -alkyl group or a phenyl group, and R2 and R3 together may form a --OC2 H4 O--, --SC2 H4 S-- or --OCH2 O-- group.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US08/779,437 US5763616A (en) | 1993-06-25 | 1997-01-07 | Indazolesulfonylurea derivative, its use and intermediate for its production |
Applications Claiming Priority (9)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP18080993 | 1993-06-25 | ||
| JP18081093 | 1993-06-25 | ||
| JP5-180809 | 1993-06-25 | ||
| JP5-180810 | 1993-06-25 | ||
| JP5-341772 | 1993-12-10 | ||
| JP34177293 | 1993-12-10 | ||
| US08/373,273 US5534481A (en) | 1993-06-25 | 1994-06-24 | Indazolesulfonylurea derivative, its use and intermediate for its production |
| US08/630,092 US5670452A (en) | 1993-06-25 | 1996-04-09 | Indazolesulfonylurea derivative, its use and intermediate for its production |
| US08/779,437 US5763616A (en) | 1993-06-25 | 1997-01-07 | Indazolesulfonylurea derivative, its use and intermediate for its production |
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| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US08/630,092 Division US5670452A (en) | 1993-06-25 | 1996-04-09 | Indazolesulfonylurea derivative, its use and intermediate for its production |
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| Publication Number | Publication Date |
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| US5763616A true US5763616A (en) | 1998-06-09 |
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| Application Number | Title | Priority Date | Filing Date |
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| US08/373,273 Expired - Fee Related US5534481A (en) | 1993-06-25 | 1994-06-24 | Indazolesulfonylurea derivative, its use and intermediate for its production |
| US08/630,092 Expired - Fee Related US5670452A (en) | 1993-06-25 | 1996-04-09 | Indazolesulfonylurea derivative, its use and intermediate for its production |
| US08/779,437 Expired - Fee Related US5763616A (en) | 1993-06-25 | 1997-01-07 | Indazolesulfonylurea derivative, its use and intermediate for its production |
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| Application Number | Title | Priority Date | Filing Date |
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| US08/373,273 Expired - Fee Related US5534481A (en) | 1993-06-25 | 1994-06-24 | Indazolesulfonylurea derivative, its use and intermediate for its production |
| US08/630,092 Expired - Fee Related US5670452A (en) | 1993-06-25 | 1996-04-09 | Indazolesulfonylurea derivative, its use and intermediate for its production |
Country Status (9)
| Country | Link |
|---|---|
| US (3) | US5534481A (en) |
| EP (1) | EP0657450B1 (en) |
| KR (1) | KR950702555A (en) |
| CN (1) | CN1048246C (en) |
| AU (1) | AU674240B2 (en) |
| BR (1) | BR9405488A (en) |
| DE (1) | DE69413183T2 (en) |
| ES (1) | ES2122290T3 (en) |
| WO (1) | WO1995000509A1 (en) |
Cited By (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20020151657A1 (en) * | 2001-04-16 | 2002-10-17 | Cohen Gordon Mark | Process for crosslinking of acrylic ester copolymers |
| US20100093724A1 (en) * | 2008-09-26 | 2010-04-15 | Boehringer Ingelheim International Gmbh | Azaindazole Compounds As CCR1 Receptor Antagonists |
| US20110034512A1 (en) * | 2008-04-29 | 2011-02-10 | Boehringer Ingelheim International Gmbh | Indazole Compounds As CCR1 Receptor Antagonists |
| US20110137042A1 (en) * | 2009-12-08 | 2011-06-09 | Boehringer Ingelheim International Gmbh | Process for Synthesis of Intermediates Useful for Making Substituted Indazole and Azaindazole Compounds |
| US20110230521A1 (en) * | 2008-05-06 | 2011-09-22 | Boehringer Ingelheim International Gmbh | Pyrazole Compounds As CCR1 Antagonists |
| US8546442B2 (en) | 2010-12-23 | 2013-10-01 | Boehringer Ingelheim International Gmbh | Pyrazolopiperidine compounds as CCR1 receptor antagonists |
| US8871786B2 (en) | 2010-04-30 | 2014-10-28 | Boehringer Ingelheim International Gmbh | Azaindazole amide compounds as CCR1 receptor antagonists |
| US8927550B2 (en) | 2009-10-27 | 2015-01-06 | Boehringer Ingelheim International Gmbh | Heterocyclic compounds as CCR1 receptor antagonists |
| US9056858B2 (en) | 2009-10-21 | 2015-06-16 | Boehringer Ingelheim International Gmbh | Indazole and pyrazolopyridine compounds as CCR1 receptor antagonists |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5872144A (en) * | 1997-02-18 | 1999-02-16 | American Home Products Corporation | 4-aminoethoxyindazole derivatives |
| JPWO2002100833A1 (en) * | 2001-06-12 | 2004-09-24 | 住友製薬株式会社 | Rho kinase inhibitor |
| US7601847B2 (en) | 2004-10-26 | 2009-10-13 | Wyeth | Preparation and purification of 4-(indazol-3-yl)phenols |
| US7820604B2 (en) * | 2006-10-27 | 2010-10-26 | Chevron Oronite Company Llc | Lubricating oil additive composition and method of making the same |
| LV14985B (en) | 2013-10-14 | 2015-06-20 | Latvijas Organiskās Sintēzes Institūts | Method for production of lenalidomide |
| CN115894478A (en) * | 2021-09-30 | 2023-04-04 | 杭州民生药物研究院有限公司 | Novel pyridopyrazole heterocyclic compound and application thereof |
Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4622062A (en) * | 1984-02-09 | 1986-11-11 | E. I. Du Pont De Nemours And Company | Herbicidal N-[(4,6-substituted pyrimidin-2-yl)aminocarbonyl]-substituted fused pyrazole-3-sulfonamides |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4465505A (en) * | 1982-01-07 | 1984-08-14 | E. I. Du Pont De Nemours And Company | Herbicidal sulfonamides |
| JPS60208978A (en) * | 1984-02-09 | 1985-10-21 | イ−・アイ・デユポン・デ・ニモアス・アンド・カンパニ− | Pyrazole sulfonylurea |
| JPH0495091A (en) * | 1990-08-10 | 1992-03-27 | Sumitomo Chem Co Ltd | Indazole sulfonamide derivative, its production and herbicide containing the derivative as active component |
| DK0673937T3 (en) * | 1993-09-10 | 2004-03-22 | Eisai Co Ltd | Bicyclic heterocyclic sulfonamide and sulfonic acid ester derivatives |
-
1994
- 1994-06-24 KR KR1019950700186A patent/KR950702555A/en not_active Application Discontinuation
- 1994-06-24 WO PCT/JP1994/001016 patent/WO1995000509A1/en active IP Right Grant
- 1994-06-24 US US08/373,273 patent/US5534481A/en not_active Expired - Fee Related
- 1994-06-24 AU AU69834/94A patent/AU674240B2/en not_active Ceased
- 1994-06-24 CN CN94190331A patent/CN1048246C/en not_active Expired - Fee Related
- 1994-06-24 EP EP94918565A patent/EP0657450B1/en not_active Expired - Lifetime
- 1994-06-24 ES ES94918565T patent/ES2122290T3/en not_active Expired - Lifetime
- 1994-06-24 BR BR9405488A patent/BR9405488A/en not_active Application Discontinuation
- 1994-06-24 DE DE69413183T patent/DE69413183T2/en not_active Expired - Fee Related
-
1996
- 1996-04-09 US US08/630,092 patent/US5670452A/en not_active Expired - Fee Related
-
1997
- 1997-01-07 US US08/779,437 patent/US5763616A/en not_active Expired - Fee Related
Patent Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4622062A (en) * | 1984-02-09 | 1986-11-11 | E. I. Du Pont De Nemours And Company | Herbicidal N-[(4,6-substituted pyrimidin-2-yl)aminocarbonyl]-substituted fused pyrazole-3-sulfonamides |
Cited By (17)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20020151657A1 (en) * | 2001-04-16 | 2002-10-17 | Cohen Gordon Mark | Process for crosslinking of acrylic ester copolymers |
| US8008327B2 (en) | 2008-04-29 | 2011-08-30 | Boehringer Ingelheim International Gmbh | Indazole compounds as CCR1 receptor antagonists |
| US8263597B2 (en) | 2008-04-29 | 2012-09-11 | Boehringer Ingelheim International Gmbh | Indazole compounds as CCR1 receptor antagonists |
| US20110034512A1 (en) * | 2008-04-29 | 2011-02-10 | Boehringer Ingelheim International Gmbh | Indazole Compounds As CCR1 Receptor Antagonists |
| US8293917B2 (en) | 2008-05-06 | 2012-10-23 | Boehringer Ingelheim International Gmbh | Pyrazole compounds as CCR1 antagonists |
| US20110230521A1 (en) * | 2008-05-06 | 2011-09-22 | Boehringer Ingelheim International Gmbh | Pyrazole Compounds As CCR1 Antagonists |
| US8063065B2 (en) | 2008-09-26 | 2011-11-22 | Boehringer Ingelheim International Gmbh | Azaindazole compounds as CCR1 receptor antagonists |
| US20110086846A1 (en) * | 2008-09-26 | 2011-04-14 | Boehringer Ingelheim International Gmbh | Azaindazole Compounds As CCR1 Receptor Antagonists |
| US8163918B2 (en) | 2008-09-26 | 2012-04-24 | Boehringer Ingelheim International Gmbh | Azaindazole compounds as CCR1 receptor antagonists |
| US7879873B2 (en) | 2008-09-26 | 2011-02-01 | Boehringer Ingelheim International Gmbh | Azaindazole compounds as CCR1 receptor antagonists |
| US20100093724A1 (en) * | 2008-09-26 | 2010-04-15 | Boehringer Ingelheim International Gmbh | Azaindazole Compounds As CCR1 Receptor Antagonists |
| US8338610B2 (en) | 2008-09-26 | 2012-12-25 | Boehringer Ingelheim International Gmbh | Pyridinyl compounds useful as intermediates |
| US9056858B2 (en) | 2009-10-21 | 2015-06-16 | Boehringer Ingelheim International Gmbh | Indazole and pyrazolopyridine compounds as CCR1 receptor antagonists |
| US8927550B2 (en) | 2009-10-27 | 2015-01-06 | Boehringer Ingelheim International Gmbh | Heterocyclic compounds as CCR1 receptor antagonists |
| US20110137042A1 (en) * | 2009-12-08 | 2011-06-09 | Boehringer Ingelheim International Gmbh | Process for Synthesis of Intermediates Useful for Making Substituted Indazole and Azaindazole Compounds |
| US8871786B2 (en) | 2010-04-30 | 2014-10-28 | Boehringer Ingelheim International Gmbh | Azaindazole amide compounds as CCR1 receptor antagonists |
| US8546442B2 (en) | 2010-12-23 | 2013-10-01 | Boehringer Ingelheim International Gmbh | Pyrazolopiperidine compounds as CCR1 receptor antagonists |
Also Published As
| Publication number | Publication date |
|---|---|
| AU681838B2 (en) | 1997-09-04 |
| AU7036096A (en) | 1997-01-09 |
| US5534481A (en) | 1996-07-09 |
| US5670452A (en) | 1997-09-23 |
| CN1048246C (en) | 2000-01-12 |
| WO1995000509A1 (en) | 1995-01-05 |
| AU674240B2 (en) | 1996-12-12 |
| EP0657450A4 (en) | 1995-12-27 |
| DE69413183T2 (en) | 1999-02-11 |
| CN1110478A (en) | 1995-10-18 |
| EP0657450B1 (en) | 1998-09-09 |
| EP0657450A1 (en) | 1995-06-14 |
| KR950702555A (en) | 1995-07-29 |
| ES2122290T3 (en) | 1998-12-16 |
| DE69413183D1 (en) | 1998-10-15 |
| AU6983494A (en) | 1995-01-17 |
| BR9405488A (en) | 1999-06-01 |
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